Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP851280.RA0xhrKtq9-qHkUlTbHcZByFtBaDYBuGF6VLtCsZXeHlE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP851280.RA0xhrKtq9-qHkUlTbHcZByFtBaDYBuGF6VLtCsZXeHlE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP851280.RA0xhrKtq9-qHkUlTbHcZByFtBaDYBuGF6VLtCsZXeHlE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP851280.RA0xhrKtq9-qHkUlTbHcZByFtBaDYBuGF6VLtCsZXeHlE130_provenance.
- NP851280.RA0xhrKtq9-qHkUlTbHcZByFtBaDYBuGF6VLtCsZXeHlE130_assertion description "[In whites, a single variant (rs1503298) in TLL1 was significantly (P=5.5 � 10(-6)) associated with extent of CAD, defined as number of lesions with percent diameter stenosis ?20%, after stringent Bonferroni correction for all 3351 single nucleotide polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP851280.RA0xhrKtq9-qHkUlTbHcZByFtBaDYBuGF6VLtCsZXeHlE130_provenance.
- NP851280.RA0xhrKtq9-qHkUlTbHcZByFtBaDYBuGF6VLtCsZXeHlE130_assertion evidence source_evidence_literature NP851280.RA0xhrKtq9-qHkUlTbHcZByFtBaDYBuGF6VLtCsZXeHlE130_provenance.
- NP851280.RA0xhrKtq9-qHkUlTbHcZByFtBaDYBuGF6VLtCsZXeHlE130_assertion SIO_000772 21911782 NP851280.RA0xhrKtq9-qHkUlTbHcZByFtBaDYBuGF6VLtCsZXeHlE130_provenance.
- NP851280.RA0xhrKtq9-qHkUlTbHcZByFtBaDYBuGF6VLtCsZXeHlE130_assertion wasDerivedFrom befree-20140225 NP851280.RA0xhrKtq9-qHkUlTbHcZByFtBaDYBuGF6VLtCsZXeHlE130_provenance.
- NP851280.RA0xhrKtq9-qHkUlTbHcZByFtBaDYBuGF6VLtCsZXeHlE130_assertion wasGeneratedBy ECO_0000203 NP851280.RA0xhrKtq9-qHkUlTbHcZByFtBaDYBuGF6VLtCsZXeHlE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP851280.RA0xhrKtq9-qHkUlTbHcZByFtBaDYBuGF6VLtCsZXeHlE130_provenance.