Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP536843.RA7q98jd5PxEg2C9pRcB8WeoKZoavFj9E8IrPYdR7TKkA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP536843.RA7q98jd5PxEg2C9pRcB8WeoKZoavFj9E8IrPYdR7TKkA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP536843.RA7q98jd5PxEg2C9pRcB8WeoKZoavFj9E8IrPYdR7TKkA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP536843.RA7q98jd5PxEg2C9pRcB8WeoKZoavFj9E8IrPYdR7TKkA130_provenance.
- NP536843.RA7q98jd5PxEg2C9pRcB8WeoKZoavFj9E8IrPYdR7TKkA130_assertion description "[Mutations in the KAL gene (Kallmann syndrome) and the AHC gene (adrenal hypoplasia congenita/HH) cause X-linked recessive HH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP536843.RA7q98jd5PxEg2C9pRcB8WeoKZoavFj9E8IrPYdR7TKkA130_provenance.
- NP536843.RA7q98jd5PxEg2C9pRcB8WeoKZoavFj9E8IrPYdR7TKkA130_assertion evidence source_evidence_literature NP536843.RA7q98jd5PxEg2C9pRcB8WeoKZoavFj9E8IrPYdR7TKkA130_provenance.
- NP536843.RA7q98jd5PxEg2C9pRcB8WeoKZoavFj9E8IrPYdR7TKkA130_assertion SIO_000772 10727999 NP536843.RA7q98jd5PxEg2C9pRcB8WeoKZoavFj9E8IrPYdR7TKkA130_provenance.
- NP536843.RA7q98jd5PxEg2C9pRcB8WeoKZoavFj9E8IrPYdR7TKkA130_assertion wasDerivedFrom befree-20140225 NP536843.RA7q98jd5PxEg2C9pRcB8WeoKZoavFj9E8IrPYdR7TKkA130_provenance.
- NP536843.RA7q98jd5PxEg2C9pRcB8WeoKZoavFj9E8IrPYdR7TKkA130_assertion wasGeneratedBy ECO_0000203 NP536843.RA7q98jd5PxEg2C9pRcB8WeoKZoavFj9E8IrPYdR7TKkA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP536843.RA7q98jd5PxEg2C9pRcB8WeoKZoavFj9E8IrPYdR7TKkA130_provenance.