Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP446639.RAkDwXHUATtxHHbCj5HgK6D-cN9PDZEQTOgpnGclRNAw4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP446639.RAkDwXHUATtxHHbCj5HgK6D-cN9PDZEQTOgpnGclRNAw4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446639.RAkDwXHUATtxHHbCj5HgK6D-cN9PDZEQTOgpnGclRNAw4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446639.RAkDwXHUATtxHHbCj5HgK6D-cN9PDZEQTOgpnGclRNAw4130_provenance.
- NP446639.RAkDwXHUATtxHHbCj5HgK6D-cN9PDZEQTOgpnGclRNAw4130_assertion description "[The CFH 402H allele was associated with an increased risk for incident CHD and ischemic stroke in whites, with the strength and significance of the association dependent upon hypertension status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446639.RAkDwXHUATtxHHbCj5HgK6D-cN9PDZEQTOgpnGclRNAw4130_provenance.
- NP446639.RAkDwXHUATtxHHbCj5HgK6D-cN9PDZEQTOgpnGclRNAw4130_assertion evidence source_evidence_literature NP446639.RAkDwXHUATtxHHbCj5HgK6D-cN9PDZEQTOgpnGclRNAw4130_provenance.
- NP446639.RAkDwXHUATtxHHbCj5HgK6D-cN9PDZEQTOgpnGclRNAw4130_assertion SIO_000772 18292760 NP446639.RAkDwXHUATtxHHbCj5HgK6D-cN9PDZEQTOgpnGclRNAw4130_provenance.
- NP446639.RAkDwXHUATtxHHbCj5HgK6D-cN9PDZEQTOgpnGclRNAw4130_assertion wasDerivedFrom befree-20150227 NP446639.RAkDwXHUATtxHHbCj5HgK6D-cN9PDZEQTOgpnGclRNAw4130_provenance.
- NP446639.RAkDwXHUATtxHHbCj5HgK6D-cN9PDZEQTOgpnGclRNAw4130_assertion wasGeneratedBy ECO_0000203 NP446639.RAkDwXHUATtxHHbCj5HgK6D-cN9PDZEQTOgpnGclRNAw4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP446639.RAkDwXHUATtxHHbCj5HgK6D-cN9PDZEQTOgpnGclRNAw4130_provenance.