Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP690066.RAb0uDOeE0gL7FnfmXT_QOdCOHb9QDo6F9_VIA-fvCCZQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP690066.RAb0uDOeE0gL7FnfmXT_QOdCOHb9QDo6F9_VIA-fvCCZQ130_assertion type Assertion NP690066.RAb0uDOeE0gL7FnfmXT_QOdCOHb9QDo6F9_VIA-fvCCZQ130_head.
- NP690066.RAb0uDOeE0gL7FnfmXT_QOdCOHb9QDo6F9_VIA-fvCCZQ130_assertion description "[The P-selectin gene is highly polymorphic: reduced frequency of the Pro715 allele carriers in patients with myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690066.RAb0uDOeE0gL7FnfmXT_QOdCOHb9QDo6F9_VIA-fvCCZQ130_provenance.
- NP690066.RAb0uDOeE0gL7FnfmXT_QOdCOHb9QDo6F9_VIA-fvCCZQ130_assertion evidence source_evidence_literature NP690066.RAb0uDOeE0gL7FnfmXT_QOdCOHb9QDo6F9_VIA-fvCCZQ130_provenance.
- NP690066.RAb0uDOeE0gL7FnfmXT_QOdCOHb9QDo6F9_VIA-fvCCZQ130_assertion SIO_000772 9668170 NP690066.RAb0uDOeE0gL7FnfmXT_QOdCOHb9QDo6F9_VIA-fvCCZQ130_provenance.
- NP690066.RAb0uDOeE0gL7FnfmXT_QOdCOHb9QDo6F9_VIA-fvCCZQ130_assertion wasDerivedFrom befree-20150227 NP690066.RAb0uDOeE0gL7FnfmXT_QOdCOHb9QDo6F9_VIA-fvCCZQ130_provenance.
- NP690066.RAb0uDOeE0gL7FnfmXT_QOdCOHb9QDo6F9_VIA-fvCCZQ130_assertion wasGeneratedBy ECO_0000203 NP690066.RAb0uDOeE0gL7FnfmXT_QOdCOHb9QDo6F9_VIA-fvCCZQ130_provenance.