Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP192885.RAeI92U3uCaX-pUVPvdBgqi2nVpWsns-L6z2J3NDcyY4w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP192885.RAeI92U3uCaX-pUVPvdBgqi2nVpWsns-L6z2J3NDcyY4w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP192885.RAeI92U3uCaX-pUVPvdBgqi2nVpWsns-L6z2J3NDcyY4w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP192885.RAeI92U3uCaX-pUVPvdBgqi2nVpWsns-L6z2J3NDcyY4w130_provenance.
- NP192885.RAeI92U3uCaX-pUVPvdBgqi2nVpWsns-L6z2J3NDcyY4w130_assertion description "[Carrying at least one copy of the variant XRCC4 allele (rs1805377) was associated with a significantly increased risk of renal cell carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP192885.RAeI92U3uCaX-pUVPvdBgqi2nVpWsns-L6z2J3NDcyY4w130_provenance.
- NP192885.RAeI92U3uCaX-pUVPvdBgqi2nVpWsns-L6z2J3NDcyY4w130_assertion evidence source_evidence_literature NP192885.RAeI92U3uCaX-pUVPvdBgqi2nVpWsns-L6z2J3NDcyY4w130_provenance.
- NP192885.RAeI92U3uCaX-pUVPvdBgqi2nVpWsns-L6z2J3NDcyY4w130_assertion SIO_000772 18768505 NP192885.RAeI92U3uCaX-pUVPvdBgqi2nVpWsns-L6z2J3NDcyY4w130_provenance.
- NP192885.RAeI92U3uCaX-pUVPvdBgqi2nVpWsns-L6z2J3NDcyY4w130_assertion wasDerivedFrom lhgdn-20090331 NP192885.RAeI92U3uCaX-pUVPvdBgqi2nVpWsns-L6z2J3NDcyY4w130_provenance.
- NP192885.RAeI92U3uCaX-pUVPvdBgqi2nVpWsns-L6z2J3NDcyY4w130_assertion wasGeneratedBy ECO_0000203 NP192885.RAeI92U3uCaX-pUVPvdBgqi2nVpWsns-L6z2J3NDcyY4w130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP192885.RAeI92U3uCaX-pUVPvdBgqi2nVpWsns-L6z2J3NDcyY4w130_provenance.