Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1011148.RA7yHTuczRK1XCWgHT5plKch9h87rmwtZZXO-30Sk3UKI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1011148.RA7yHTuczRK1XCWgHT5plKch9h87rmwtZZXO-30Sk3UKI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1011148.RA7yHTuczRK1XCWgHT5plKch9h87rmwtZZXO-30Sk3UKI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1011148.RA7yHTuczRK1XCWgHT5plKch9h87rmwtZZXO-30Sk3UKI130_provenance.
- NP1011148.RA7yHTuczRK1XCWgHT5plKch9h87rmwtZZXO-30Sk3UKI130_assertion description "[Seventeen out of 38 (45%) patients with STEMI were homozygous for the HPA-3 b allele compared to 6 out 62 (10%) with NSTEMI-UA , 4 out of 18 (22%) with chronic CAD and 2 out of 15 (13%) healthy controls (chi(2)=16,4, p=0.03.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011148.RA7yHTuczRK1XCWgHT5plKch9h87rmwtZZXO-30Sk3UKI130_provenance.
- NP1011148.RA7yHTuczRK1XCWgHT5plKch9h87rmwtZZXO-30Sk3UKI130_assertion evidence source_evidence_literature NP1011148.RA7yHTuczRK1XCWgHT5plKch9h87rmwtZZXO-30Sk3UKI130_provenance.
- NP1011148.RA7yHTuczRK1XCWgHT5plKch9h87rmwtZZXO-30Sk3UKI130_assertion SIO_000772 17561290 NP1011148.RA7yHTuczRK1XCWgHT5plKch9h87rmwtZZXO-30Sk3UKI130_provenance.
- NP1011148.RA7yHTuczRK1XCWgHT5plKch9h87rmwtZZXO-30Sk3UKI130_assertion wasDerivedFrom befree-20150227 NP1011148.RA7yHTuczRK1XCWgHT5plKch9h87rmwtZZXO-30Sk3UKI130_provenance.
- NP1011148.RA7yHTuczRK1XCWgHT5plKch9h87rmwtZZXO-30Sk3UKI130_assertion wasGeneratedBy ECO_0000203 NP1011148.RA7yHTuczRK1XCWgHT5plKch9h87rmwtZZXO-30Sk3UKI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1011148.RA7yHTuczRK1XCWgHT5plKch9h87rmwtZZXO-30Sk3UKI130_provenance.