Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP968328.RAQuHB4q2h_44tPSP5QSLAKf1Hk48tvHY7LAfOVrMUx6U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP968328.RAQuHB4q2h_44tPSP5QSLAKf1Hk48tvHY7LAfOVrMUx6U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP968328.RAQuHB4q2h_44tPSP5QSLAKf1Hk48tvHY7LAfOVrMUx6U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP968328.RAQuHB4q2h_44tPSP5QSLAKf1Hk48tvHY7LAfOVrMUx6U130_provenance.
- NP968328.RAQuHB4q2h_44tPSP5QSLAKf1Hk48tvHY7LAfOVrMUx6U130_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." NP968328.RAQuHB4q2h_44tPSP5QSLAKf1Hk48tvHY7LAfOVrMUx6U130_provenance.
- NP968328.RAQuHB4q2h_44tPSP5QSLAKf1Hk48tvHY7LAfOVrMUx6U130_assertion evidence source_evidence_literature NP968328.RAQuHB4q2h_44tPSP5QSLAKf1Hk48tvHY7LAfOVrMUx6U130_provenance.
- NP968328.RAQuHB4q2h_44tPSP5QSLAKf1Hk48tvHY7LAfOVrMUx6U130_assertion SIO_000772 17561290 NP968328.RAQuHB4q2h_44tPSP5QSLAKf1Hk48tvHY7LAfOVrMUx6U130_provenance.
- NP968328.RAQuHB4q2h_44tPSP5QSLAKf1Hk48tvHY7LAfOVrMUx6U130_assertion wasDerivedFrom befree-20150227 NP968328.RAQuHB4q2h_44tPSP5QSLAKf1Hk48tvHY7LAfOVrMUx6U130_provenance.
- NP968328.RAQuHB4q2h_44tPSP5QSLAKf1Hk48tvHY7LAfOVrMUx6U130_assertion wasGeneratedBy ECO_0000203 NP968328.RAQuHB4q2h_44tPSP5QSLAKf1Hk48tvHY7LAfOVrMUx6U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP968328.RAQuHB4q2h_44tPSP5QSLAKf1Hk48tvHY7LAfOVrMUx6U130_provenance.