Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP769857.RAnh6EBkTr3X6hlmcj6gBn8w6pTcHuatPg5b05-obAFfo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP769857.RAnh6EBkTr3X6hlmcj6gBn8w6pTcHuatPg5b05-obAFfo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP769857.RAnh6EBkTr3X6hlmcj6gBn8w6pTcHuatPg5b05-obAFfo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP769857.RAnh6EBkTr3X6hlmcj6gBn8w6pTcHuatPg5b05-obAFfo130_provenance.
- NP769857.RAnh6EBkTr3X6hlmcj6gBn8w6pTcHuatPg5b05-obAFfo130_assertion description "[Mutations in the GLI-similar 3 (GLIS3) gene encoding the transcription factor GLIS3 are a rare cause of neonatal diabetes and congenital hypothyroidism with six affected cases from three families reported to date.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP769857.RAnh6EBkTr3X6hlmcj6gBn8w6pTcHuatPg5b05-obAFfo130_provenance.
- NP769857.RAnh6EBkTr3X6hlmcj6gBn8w6pTcHuatPg5b05-obAFfo130_assertion evidence source_evidence_literature NP769857.RAnh6EBkTr3X6hlmcj6gBn8w6pTcHuatPg5b05-obAFfo130_provenance.
- NP769857.RAnh6EBkTr3X6hlmcj6gBn8w6pTcHuatPg5b05-obAFfo130_assertion SIO_000772 21139041 NP769857.RAnh6EBkTr3X6hlmcj6gBn8w6pTcHuatPg5b05-obAFfo130_provenance.
- NP769857.RAnh6EBkTr3X6hlmcj6gBn8w6pTcHuatPg5b05-obAFfo130_assertion wasDerivedFrom befree-20140225 NP769857.RAnh6EBkTr3X6hlmcj6gBn8w6pTcHuatPg5b05-obAFfo130_provenance.
- NP769857.RAnh6EBkTr3X6hlmcj6gBn8w6pTcHuatPg5b05-obAFfo130_assertion wasGeneratedBy ECO_0000203 NP769857.RAnh6EBkTr3X6hlmcj6gBn8w6pTcHuatPg5b05-obAFfo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP769857.RAnh6EBkTr3X6hlmcj6gBn8w6pTcHuatPg5b05-obAFfo130_provenance.