Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP809668.RA2fR_v0R5bcmGBst3hFaf067UdQCDI90VYAQW0KD4xlM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP809668.RA2fR_v0R5bcmGBst3hFaf067UdQCDI90VYAQW0KD4xlM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP809668.RA2fR_v0R5bcmGBst3hFaf067UdQCDI90VYAQW0KD4xlM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP809668.RA2fR_v0R5bcmGBst3hFaf067UdQCDI90VYAQW0KD4xlM130_provenance.
- befree-2016 importedOn "2016-02-19" NP809668.RA2fR_v0R5bcmGBst3hFaf067UdQCDI90VYAQW0KD4xlM130_provenance.
- NP809668.RA2fR_v0R5bcmGBst3hFaf067UdQCDI90VYAQW0KD4xlM130_assertion wasGeneratedBy ECO_0000203 NP809668.RA2fR_v0R5bcmGBst3hFaf067UdQCDI90VYAQW0KD4xlM130_provenance.
- NP809668.RA2fR_v0R5bcmGBst3hFaf067UdQCDI90VYAQW0KD4xlM130_assertion wasDerivedFrom befree-2016 NP809668.RA2fR_v0R5bcmGBst3hFaf067UdQCDI90VYAQW0KD4xlM130_provenance.
- NP809668.RA2fR_v0R5bcmGBst3hFaf067UdQCDI90VYAQW0KD4xlM130_assertion SIO_000772 20436471 NP809668.RA2fR_v0R5bcmGBst3hFaf067UdQCDI90VYAQW0KD4xlM130_provenance.
- NP809668.RA2fR_v0R5bcmGBst3hFaf067UdQCDI90VYAQW0KD4xlM130_assertion evidence source_evidence_literature NP809668.RA2fR_v0R5bcmGBst3hFaf067UdQCDI90VYAQW0KD4xlM130_provenance.
- NP809668.RA2fR_v0R5bcmGBst3hFaf067UdQCDI90VYAQW0KD4xlM130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809668.RA2fR_v0R5bcmGBst3hFaf067UdQCDI90VYAQW0KD4xlM130_provenance.