Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP442565.RAne_9XaZDXC1EpEa5ZwQetRxjWTWpbfmpwGM-VMmkg1I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP442565.RAne_9XaZDXC1EpEa5ZwQetRxjWTWpbfmpwGM-VMmkg1I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP442565.RAne_9XaZDXC1EpEa5ZwQetRxjWTWpbfmpwGM-VMmkg1I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP442565.RAne_9XaZDXC1EpEa5ZwQetRxjWTWpbfmpwGM-VMmkg1I130_provenance.
- NP442565.RAne_9XaZDXC1EpEa5ZwQetRxjWTWpbfmpwGM-VMmkg1I130_assertion description "[Mutations in the Timp-3 gene cause Sorsby fundus dystrophy (SFD), a hereditary macular degenerative disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP442565.RAne_9XaZDXC1EpEa5ZwQetRxjWTWpbfmpwGM-VMmkg1I130_provenance.
- NP442565.RAne_9XaZDXC1EpEa5ZwQetRxjWTWpbfmpwGM-VMmkg1I130_assertion evidence source_evidence_literature NP442565.RAne_9XaZDXC1EpEa5ZwQetRxjWTWpbfmpwGM-VMmkg1I130_provenance.
- NP442565.RAne_9XaZDXC1EpEa5ZwQetRxjWTWpbfmpwGM-VMmkg1I130_assertion SIO_000772 15123717 NP442565.RAne_9XaZDXC1EpEa5ZwQetRxjWTWpbfmpwGM-VMmkg1I130_provenance.
- NP442565.RAne_9XaZDXC1EpEa5ZwQetRxjWTWpbfmpwGM-VMmkg1I130_assertion wasDerivedFrom befree-2016 NP442565.RAne_9XaZDXC1EpEa5ZwQetRxjWTWpbfmpwGM-VMmkg1I130_provenance.
- NP442565.RAne_9XaZDXC1EpEa5ZwQetRxjWTWpbfmpwGM-VMmkg1I130_assertion wasGeneratedBy ECO_0000203 NP442565.RAne_9XaZDXC1EpEa5ZwQetRxjWTWpbfmpwGM-VMmkg1I130_provenance.
- befree-2016 importedOn "2016-02-19" NP442565.RAne_9XaZDXC1EpEa5ZwQetRxjWTWpbfmpwGM-VMmkg1I130_provenance.