Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP379743.RAaIBJ3xLyAnRa6gdRZ3wtV3ic0NHXgOv6TX6okx4k_CA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP379743.RAaIBJ3xLyAnRa6gdRZ3wtV3ic0NHXgOv6TX6okx4k_CA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP379743.RAaIBJ3xLyAnRa6gdRZ3wtV3ic0NHXgOv6TX6okx4k_CA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP379743.RAaIBJ3xLyAnRa6gdRZ3wtV3ic0NHXgOv6TX6okx4k_CA130_provenance.
- NP379743.RAaIBJ3xLyAnRa6gdRZ3wtV3ic0NHXgOv6TX6okx4k_CA130_assertion description "[In this study we examined whether polymorphisms in GST genes influence the risk of CAD in a case-control group of South Asians, following our recent observation of such an association in Caucasians from the same region of the UK.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP379743.RAaIBJ3xLyAnRa6gdRZ3wtV3ic0NHXgOv6TX6okx4k_CA130_provenance.
- NP379743.RAaIBJ3xLyAnRa6gdRZ3wtV3ic0NHXgOv6TX6okx4k_CA130_assertion evidence source_evidence_literature NP379743.RAaIBJ3xLyAnRa6gdRZ3wtV3ic0NHXgOv6TX6okx4k_CA130_provenance.
- NP379743.RAaIBJ3xLyAnRa6gdRZ3wtV3ic0NHXgOv6TX6okx4k_CA130_assertion SIO_000772 12519635 NP379743.RAaIBJ3xLyAnRa6gdRZ3wtV3ic0NHXgOv6TX6okx4k_CA130_provenance.
- NP379743.RAaIBJ3xLyAnRa6gdRZ3wtV3ic0NHXgOv6TX6okx4k_CA130_assertion wasDerivedFrom befree-2016 NP379743.RAaIBJ3xLyAnRa6gdRZ3wtV3ic0NHXgOv6TX6okx4k_CA130_provenance.
- NP379743.RAaIBJ3xLyAnRa6gdRZ3wtV3ic0NHXgOv6TX6okx4k_CA130_assertion wasGeneratedBy ECO_0000203 NP379743.RAaIBJ3xLyAnRa6gdRZ3wtV3ic0NHXgOv6TX6okx4k_CA130_provenance.
- befree-2016 importedOn "2016-02-19" NP379743.RAaIBJ3xLyAnRa6gdRZ3wtV3ic0NHXgOv6TX6okx4k_CA130_provenance.