Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1216497.RArVUrEsg-qckMNLAX4UJPvqE8n3sIz0cxZIPIGOGDVIs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1216497.RArVUrEsg-qckMNLAX4UJPvqE8n3sIz0cxZIPIGOGDVIs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1216497.RArVUrEsg-qckMNLAX4UJPvqE8n3sIz0cxZIPIGOGDVIs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1216497.RArVUrEsg-qckMNLAX4UJPvqE8n3sIz0cxZIPIGOGDVIs130_provenance.
- NP1216497.RArVUrEsg-qckMNLAX4UJPvqE8n3sIz0cxZIPIGOGDVIs130_assertion description "[Early findings suggested that rare and low-frequency coding variation might have a large effect on human phenotypes (eg, PCSK9 missense variants on low-density lipoprotein-cholesterol and coronary heart diseases).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216497.RArVUrEsg-qckMNLAX4UJPvqE8n3sIz0cxZIPIGOGDVIs130_provenance.
- NP1216497.RArVUrEsg-qckMNLAX4UJPvqE8n3sIz0cxZIPIGOGDVIs130_assertion evidence source_evidence_literature NP1216497.RArVUrEsg-qckMNLAX4UJPvqE8n3sIz0cxZIPIGOGDVIs130_provenance.
- NP1216497.RArVUrEsg-qckMNLAX4UJPvqE8n3sIz0cxZIPIGOGDVIs130_assertion SIO_000772 25185437 NP1216497.RArVUrEsg-qckMNLAX4UJPvqE8n3sIz0cxZIPIGOGDVIs130_provenance.
- NP1216497.RArVUrEsg-qckMNLAX4UJPvqE8n3sIz0cxZIPIGOGDVIs130_assertion wasDerivedFrom befree-2016 NP1216497.RArVUrEsg-qckMNLAX4UJPvqE8n3sIz0cxZIPIGOGDVIs130_provenance.
- NP1216497.RArVUrEsg-qckMNLAX4UJPvqE8n3sIz0cxZIPIGOGDVIs130_assertion wasGeneratedBy ECO_0000203 NP1216497.RArVUrEsg-qckMNLAX4UJPvqE8n3sIz0cxZIPIGOGDVIs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1216497.RArVUrEsg-qckMNLAX4UJPvqE8n3sIz0cxZIPIGOGDVIs130_provenance.