Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP518012.RAPfun-6nttt1CWnEEA26_VcfPgJPzSSKGkkHkapVNSfk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP518012.RAPfun-6nttt1CWnEEA26_VcfPgJPzSSKGkkHkapVNSfk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP518012.RAPfun-6nttt1CWnEEA26_VcfPgJPzSSKGkkHkapVNSfk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP518012.RAPfun-6nttt1CWnEEA26_VcfPgJPzSSKGkkHkapVNSfk130_provenance.
- NP518012.RAPfun-6nttt1CWnEEA26_VcfPgJPzSSKGkkHkapVNSfk130_assertion description "[The enhanced P-selection expression in MBTS-operated CCHD children and reduced GPIb expression in non-MBTS patients, especially in younger patients, were positively associated with the occurrence of the polymorphic variant Pl(A2) of platelet membrane glycoprotein IIIa gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518012.RAPfun-6nttt1CWnEEA26_VcfPgJPzSSKGkkHkapVNSfk130_provenance.
- NP518012.RAPfun-6nttt1CWnEEA26_VcfPgJPzSSKGkkHkapVNSfk130_assertion evidence source_evidence_literature NP518012.RAPfun-6nttt1CWnEEA26_VcfPgJPzSSKGkkHkapVNSfk130_provenance.
- NP518012.RAPfun-6nttt1CWnEEA26_VcfPgJPzSSKGkkHkapVNSfk130_assertion SIO_000772 11399341 NP518012.RAPfun-6nttt1CWnEEA26_VcfPgJPzSSKGkkHkapVNSfk130_provenance.
- NP518012.RAPfun-6nttt1CWnEEA26_VcfPgJPzSSKGkkHkapVNSfk130_assertion wasDerivedFrom befree-20150227 NP518012.RAPfun-6nttt1CWnEEA26_VcfPgJPzSSKGkkHkapVNSfk130_provenance.
- NP518012.RAPfun-6nttt1CWnEEA26_VcfPgJPzSSKGkkHkapVNSfk130_assertion wasGeneratedBy ECO_0000203 NP518012.RAPfun-6nttt1CWnEEA26_VcfPgJPzSSKGkkHkapVNSfk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP518012.RAPfun-6nttt1CWnEEA26_VcfPgJPzSSKGkkHkapVNSfk130_provenance.