replace disease -> genetic disorder

nf_research_tools.rdb.model.csv

@@ -104,7 +104,7 @@ strProfile,Short tandem repeat profile information.,,,FALSE,,cellLineDetails,,,
 populationDoublingTime,Time for cell line to double,,,FALSE,,cellLineDetails,,,
 resistance,List of compounds if a cell line has been selected for.,,,FALSE,,cellLineDetails,,,list like
 contaminatedMisidentified,If a cell line has been contaminated or misidentified,,,FALSE,,cellLineDetails,,,
-cellLineGeneticDisorder,"Genetic diseases are diseases in which inherited genes predispose to increased risk. The genetic disorders associated with cancer often result from an alteration or mutation in a single gene. The diseases range from rare dominant cancer family syndrome to familial tendencies in which low-penetrance genes may interact with other genes or environmental factors to induce cancer. Research may involve clinical, epidemiologic, and laboratory studies of persons, families, and populations at high risk of these disorders. [ NCI ]","Neurofibromatosis type 1, Neurofibromatosis type 2, Schwannomatosis, No known disease",,FALSE,http://purl.obolibrary.org/obo/NCIT_C3101,cellLineDetails,,,list like
+cellLineGeneticDisorder,"Genetic diseases are diseases in which inherited genes predispose to increased risk. The genetic disorders associated with cancer often result from an alteration or mutation in a single gene. The diseases range from rare dominant cancer family syndrome to familial tendencies in which low-penetrance genes may interact with other genes or environmental factors to induce cancer. Research may involve clinical, epidemiologic, and laboratory studies of persons, families, and populations at high risk of these disorders. [ NCI ]","Neurofibromatosis type 1, Neurofibromatosis type 2, Schwannomatosis, No known genetic disorder",,FALSE,http://purl.obolibrary.org/obo/NCIT_C3101,cellLineDetails,,,list like
 cellLineManifestation,"Manifestations/symptoms that this resource is used to model (e.g. tumor type, behavioral phenotype, etc.)",,,FALSE,,cellLineDetails,,,list like
 mutationDetails,"The changing of the structure of a gene, resulting in a variant form that may be transmitted to subsequent generations",,"Component, mutationDetailsId, externalMutationID, alleleType, mutationType, mutationMethod, affectedGeneSymbol, affectedGeneName, sequenceVariation, proteinVariation, animalModelMutation, humanClinVarMutation, chromosome",FALSE,,mutationDetails,"mutationDetailsId, externalMutationID, alleleType, mutationType, mutationMethod, affectedGeneSymbol, affectedGeneName, sequenceVariation, proteinVariation, animalModelMutation, humanClinVarMutation, chromosome",,
 mutationDetailsId,A unique identifier for mutation.,,,FALSE,,mutationDetails,,,
@@ -130,7 +130,7 @@ strainNomenclature,The standard nomenclature for the strain. (e.g. B6.129S2-NF1t
 generation,The generation of the animal model. (e.g. 13),,,FALSE,,animalModelDetails,,,
 transplantationType,"Type of transplantation involved in the experiment, derived from MESH","allograft, xenograft, autograft, isograft",,FALSE,,animalModelDetails,,,
 transplantationDonorId,The donor indentifier number for the transplantion donor. ,,donorId,FALSE,,animalModelDetails,,,
-animalModelGeneticDisorder,"Genetic diseases are diseases in which inherited genes predispose to increased risk. The genetic disorders associated with cancer often result from an alteration or mutation in a single gene. The diseases range from rare dominant cancer family syndrome to familial tendencies in which low-penetrance genes may interact with other genes or environmental factors to induce cancer. Research may involve clinical, epidemiologic, and laboratory studies of persons, families, and populations at high risk of these disorders. [ NCI ]","Neurofibromatosis type 1, Neurofibromatosis type 2, Schwannomatosis, No known disease",,TRUE,http://purl.obolibrary.org/obo/NCIT_C3101,animalModelDetails,,,list
+animalModelGeneticDisorder,"Genetic diseases are diseases in which inherited genes predispose to increased risk. The genetic disorders associated with cancer often result from an alteration or mutation in a single gene. The diseases range from rare dominant cancer family syndrome to familial tendencies in which low-penetrance genes may interact with other genes or environmental factors to induce cancer. Research may involve clinical, epidemiologic, and laboratory studies of persons, families, and populations at high risk of these disorders. [ NCI ]","Neurofibromatosis type 1, Neurofibromatosis type 2, Schwannomatosis, No known genetic disorder",,TRUE,http://purl.obolibrary.org/obo/NCIT_C3101,animalModelDetails,,,list
 animalModelOfManifestation,"Manifestations/symptoms that this resource is used to model (e.g. tumor type, behavioral phenotype, etc.) ",,,TRUE,,animalModelDetails,,,list like
 development,"resourceId, investigatorId, publicationId, funderId (intermediary table)",,"Component, developmentId, resourceId, investigatorId, publicationId, funderId",FALSE,,development,"developmentId, resourceId, investigatorId, publicationId, funderId","resource, investigator, publication, funder",
 developmentId,A unique identifier for the development of the resource.,,,TRUE,,development,,,