Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP775516.RA7hkOW1C77aIcKCP6sFJLnQvUvdreRRhmnTfTQmgHKfk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP775516.RA7hkOW1C77aIcKCP6sFJLnQvUvdreRRhmnTfTQmgHKfk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP775516.RA7hkOW1C77aIcKCP6sFJLnQvUvdreRRhmnTfTQmgHKfk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP775516.RA7hkOW1C77aIcKCP6sFJLnQvUvdreRRhmnTfTQmgHKfk130_provenance.
- NP775516.RA7hkOW1C77aIcKCP6sFJLnQvUvdreRRhmnTfTQmgHKfk130_assertion description "[The USF1 variant rs2516839, associated previously with atherosclerotic lesions, showed an effect on TGs in members of the dyslipidemic families with documented coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775516.RA7hkOW1C77aIcKCP6sFJLnQvUvdreRRhmnTfTQmgHKfk130_provenance.
- NP775516.RA7hkOW1C77aIcKCP6sFJLnQvUvdreRRhmnTfTQmgHKfk130_assertion evidence source_evidence_literature NP775516.RA7hkOW1C77aIcKCP6sFJLnQvUvdreRRhmnTfTQmgHKfk130_provenance.
- NP775516.RA7hkOW1C77aIcKCP6sFJLnQvUvdreRRhmnTfTQmgHKfk130_assertion SIO_000772 19910639 NP775516.RA7hkOW1C77aIcKCP6sFJLnQvUvdreRRhmnTfTQmgHKfk130_provenance.
- NP775516.RA7hkOW1C77aIcKCP6sFJLnQvUvdreRRhmnTfTQmgHKfk130_assertion wasDerivedFrom befree-2016 NP775516.RA7hkOW1C77aIcKCP6sFJLnQvUvdreRRhmnTfTQmgHKfk130_provenance.
- NP775516.RA7hkOW1C77aIcKCP6sFJLnQvUvdreRRhmnTfTQmgHKfk130_assertion wasGeneratedBy ECO_0000203 NP775516.RA7hkOW1C77aIcKCP6sFJLnQvUvdreRRhmnTfTQmgHKfk130_provenance.
- befree-2016 importedOn "2016-02-19" NP775516.RA7hkOW1C77aIcKCP6sFJLnQvUvdreRRhmnTfTQmgHKfk130_provenance.