Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP618079.RAX_WEcTL8b7UpXvjKrNSqqHuajDTuB0KScdLL-sruxOM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP618079.RAX_WEcTL8b7UpXvjKrNSqqHuajDTuB0KScdLL-sruxOM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP618079.RAX_WEcTL8b7UpXvjKrNSqqHuajDTuB0KScdLL-sruxOM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP618079.RAX_WEcTL8b7UpXvjKrNSqqHuajDTuB0KScdLL-sruxOM130_provenance.
- NP618079.RAX_WEcTL8b7UpXvjKrNSqqHuajDTuB0KScdLL-sruxOM130_assertion description "[Children of MAP patients have an increased risk of inheriting two MUTYH mutations compared to the general population, implicating an increased risk for developing CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618079.RAX_WEcTL8b7UpXvjKrNSqqHuajDTuB0KScdLL-sruxOM130_provenance.
- NP618079.RAX_WEcTL8b7UpXvjKrNSqqHuajDTuB0KScdLL-sruxOM130_assertion evidence source_evidence_literature NP618079.RAX_WEcTL8b7UpXvjKrNSqqHuajDTuB0KScdLL-sruxOM130_provenance.
- NP618079.RAX_WEcTL8b7UpXvjKrNSqqHuajDTuB0KScdLL-sruxOM130_assertion SIO_000772 17605803 NP618079.RAX_WEcTL8b7UpXvjKrNSqqHuajDTuB0KScdLL-sruxOM130_provenance.
- NP618079.RAX_WEcTL8b7UpXvjKrNSqqHuajDTuB0KScdLL-sruxOM130_assertion wasDerivedFrom befree-2016 NP618079.RAX_WEcTL8b7UpXvjKrNSqqHuajDTuB0KScdLL-sruxOM130_provenance.
- NP618079.RAX_WEcTL8b7UpXvjKrNSqqHuajDTuB0KScdLL-sruxOM130_assertion wasGeneratedBy ECO_0000203 NP618079.RAX_WEcTL8b7UpXvjKrNSqqHuajDTuB0KScdLL-sruxOM130_provenance.
- befree-2016 importedOn "2016-02-19" NP618079.RAX_WEcTL8b7UpXvjKrNSqqHuajDTuB0KScdLL-sruxOM130_provenance.