Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP614543.RAPbOKbhxUcUeVFu50we0TiRxM90YGr45QzOZP4qfCpWE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP614543.RAPbOKbhxUcUeVFu50we0TiRxM90YGr45QzOZP4qfCpWE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP614543.RAPbOKbhxUcUeVFu50we0TiRxM90YGr45QzOZP4qfCpWE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP614543.RAPbOKbhxUcUeVFu50we0TiRxM90YGr45QzOZP4qfCpWE130_provenance.
- NP614543.RAPbOKbhxUcUeVFu50we0TiRxM90YGr45QzOZP4qfCpWE130_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." NP614543.RAPbOKbhxUcUeVFu50we0TiRxM90YGr45QzOZP4qfCpWE130_provenance.
- NP614543.RAPbOKbhxUcUeVFu50we0TiRxM90YGr45QzOZP4qfCpWE130_assertion evidence source_evidence_literature NP614543.RAPbOKbhxUcUeVFu50we0TiRxM90YGr45QzOZP4qfCpWE130_provenance.
- NP614543.RAPbOKbhxUcUeVFu50we0TiRxM90YGr45QzOZP4qfCpWE130_assertion SIO_000772 17561290 NP614543.RAPbOKbhxUcUeVFu50we0TiRxM90YGr45QzOZP4qfCpWE130_provenance.
- NP614543.RAPbOKbhxUcUeVFu50we0TiRxM90YGr45QzOZP4qfCpWE130_assertion wasDerivedFrom befree-2016 NP614543.RAPbOKbhxUcUeVFu50we0TiRxM90YGr45QzOZP4qfCpWE130_provenance.
- NP614543.RAPbOKbhxUcUeVFu50we0TiRxM90YGr45QzOZP4qfCpWE130_assertion wasGeneratedBy ECO_0000203 NP614543.RAPbOKbhxUcUeVFu50we0TiRxM90YGr45QzOZP4qfCpWE130_provenance.
- befree-2016 importedOn "2016-02-19" NP614543.RAPbOKbhxUcUeVFu50we0TiRxM90YGr45QzOZP4qfCpWE130_provenance.