Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP108305.RAlF9CNTYXNSCcWhIwrhRl461R0uSPwndfCzYV1Iad1cI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP108305.RAlF9CNTYXNSCcWhIwrhRl461R0uSPwndfCzYV1Iad1cI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP108305.RAlF9CNTYXNSCcWhIwrhRl461R0uSPwndfCzYV1Iad1cI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP108305.RAlF9CNTYXNSCcWhIwrhRl461R0uSPwndfCzYV1Iad1cI130_provenance.
- NP108305.RAlF9CNTYXNSCcWhIwrhRl461R0uSPwndfCzYV1Iad1cI130_assertion description "[The LPL S447X polymorphism also impacts on CHD risk through interaction with hypertension, and there was an additive action of these 2 polymorphisms and SBP on CHD risk (hazard ratio for 1 SD increase in SBP for combined genotypes 1.78 1.30 to 2.45).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP108305.RAlF9CNTYXNSCcWhIwrhRl461R0uSPwndfCzYV1Iad1cI130_provenance.
- NP108305.RAlF9CNTYXNSCcWhIwrhRl461R0uSPwndfCzYV1Iad1cI130_assertion evidence source_evidence_literature NP108305.RAlF9CNTYXNSCcWhIwrhRl461R0uSPwndfCzYV1Iad1cI130_provenance.
- NP108305.RAlF9CNTYXNSCcWhIwrhRl461R0uSPwndfCzYV1Iad1cI130_assertion SIO_000772 17562973 NP108305.RAlF9CNTYXNSCcWhIwrhRl461R0uSPwndfCzYV1Iad1cI130_provenance.
- NP108305.RAlF9CNTYXNSCcWhIwrhRl461R0uSPwndfCzYV1Iad1cI130_assertion wasDerivedFrom gad-20150221 NP108305.RAlF9CNTYXNSCcWhIwrhRl461R0uSPwndfCzYV1Iad1cI130_provenance.
- NP108305.RAlF9CNTYXNSCcWhIwrhRl461R0uSPwndfCzYV1Iad1cI130_assertion wasGeneratedBy ECO_0000203 NP108305.RAlF9CNTYXNSCcWhIwrhRl461R0uSPwndfCzYV1Iad1cI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP108305.RAlF9CNTYXNSCcWhIwrhRl461R0uSPwndfCzYV1Iad1cI130_provenance.