Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP658826.RA300lWP1hPOVbuuhcrGMEgdJqnu8IU2NHhxSZdKaCvoI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP658826.RA300lWP1hPOVbuuhcrGMEgdJqnu8IU2NHhxSZdKaCvoI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP658826.RA300lWP1hPOVbuuhcrGMEgdJqnu8IU2NHhxSZdKaCvoI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP658826.RA300lWP1hPOVbuuhcrGMEgdJqnu8IU2NHhxSZdKaCvoI130_provenance.
- NP658826.RA300lWP1hPOVbuuhcrGMEgdJqnu8IU2NHhxSZdKaCvoI130_assertion description "[Haplotype B in the ALOX5AP gene was associated with an increased risk of MI in the German population, confirming previously reported associations of this haplotype with CAD (coronary artery disease) in populations from Scotland and Italy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658826.RA300lWP1hPOVbuuhcrGMEgdJqnu8IU2NHhxSZdKaCvoI130_provenance.
- NP658826.RA300lWP1hPOVbuuhcrGMEgdJqnu8IU2NHhxSZdKaCvoI130_assertion evidence source_evidence_literature NP658826.RA300lWP1hPOVbuuhcrGMEgdJqnu8IU2NHhxSZdKaCvoI130_provenance.
- NP658826.RA300lWP1hPOVbuuhcrGMEgdJqnu8IU2NHhxSZdKaCvoI130_assertion SIO_000772 18318662 NP658826.RA300lWP1hPOVbuuhcrGMEgdJqnu8IU2NHhxSZdKaCvoI130_provenance.
- NP658826.RA300lWP1hPOVbuuhcrGMEgdJqnu8IU2NHhxSZdKaCvoI130_assertion wasDerivedFrom befree-2016 NP658826.RA300lWP1hPOVbuuhcrGMEgdJqnu8IU2NHhxSZdKaCvoI130_provenance.
- NP658826.RA300lWP1hPOVbuuhcrGMEgdJqnu8IU2NHhxSZdKaCvoI130_assertion wasGeneratedBy ECO_0000203 NP658826.RA300lWP1hPOVbuuhcrGMEgdJqnu8IU2NHhxSZdKaCvoI130_provenance.
- befree-2016 importedOn "2016-02-19" NP658826.RA300lWP1hPOVbuuhcrGMEgdJqnu8IU2NHhxSZdKaCvoI130_provenance.