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- source_evidence_literature type ECO_0000212 NP259738.RAqn3yQw75PoSlfd2czXn_EXHAhLYkNPmR3lmHu_xWVRo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP259738.RAqn3yQw75PoSlfd2czXn_EXHAhLYkNPmR3lmHu_xWVRo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP259738.RAqn3yQw75PoSlfd2czXn_EXHAhLYkNPmR3lmHu_xWVRo130_provenance.
- NP259738.RAqn3yQw75PoSlfd2czXn_EXHAhLYkNPmR3lmHu_xWVRo130_assertion description "[BBS2 is a clinically and genetically heterogeneous group of disorders resulting in rod-cone dystrophy, obesity, postaxial polydactyly, renal dysfunction, and mental retardation, which were very recently associated with a novel gene designated BBS2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259738.RAqn3yQw75PoSlfd2czXn_EXHAhLYkNPmR3lmHu_xWVRo130_provenance.
- NP259738.RAqn3yQw75PoSlfd2czXn_EXHAhLYkNPmR3lmHu_xWVRo130_assertion evidence source_evidence_literature NP259738.RAqn3yQw75PoSlfd2czXn_EXHAhLYkNPmR3lmHu_xWVRo130_provenance.
- NP259738.RAqn3yQw75PoSlfd2czXn_EXHAhLYkNPmR3lmHu_xWVRo130_assertion SIO_000772 11707781 NP259738.RAqn3yQw75PoSlfd2czXn_EXHAhLYkNPmR3lmHu_xWVRo130_provenance.
- NP259738.RAqn3yQw75PoSlfd2czXn_EXHAhLYkNPmR3lmHu_xWVRo130_assertion wasDerivedFrom befree-20150227 NP259738.RAqn3yQw75PoSlfd2czXn_EXHAhLYkNPmR3lmHu_xWVRo130_provenance.
- NP259738.RAqn3yQw75PoSlfd2czXn_EXHAhLYkNPmR3lmHu_xWVRo130_assertion wasGeneratedBy ECO_0000203 NP259738.RAqn3yQw75PoSlfd2czXn_EXHAhLYkNPmR3lmHu_xWVRo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP259738.RAqn3yQw75PoSlfd2czXn_EXHAhLYkNPmR3lmHu_xWVRo130_provenance.