Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP690528.RAVLHgQtnzm4u14PIgNypeITteG4p_QyXYxlUHOJrIj6o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP690528.RAVLHgQtnzm4u14PIgNypeITteG4p_QyXYxlUHOJrIj6o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690528.RAVLHgQtnzm4u14PIgNypeITteG4p_QyXYxlUHOJrIj6o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690528.RAVLHgQtnzm4u14PIgNypeITteG4p_QyXYxlUHOJrIj6o130_provenance.
- NP690528.RAVLHgQtnzm4u14PIgNypeITteG4p_QyXYxlUHOJrIj6o130_assertion description "[Haplotypes A1 and A3 in the endothelial protein C receptor gene are tagged by the 4678G/C and 4600A/G polymorphisms, respectively, and have been reported to influence the risk of venous thromboembolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690528.RAVLHgQtnzm4u14PIgNypeITteG4p_QyXYxlUHOJrIj6o130_provenance.
- NP690528.RAVLHgQtnzm4u14PIgNypeITteG4p_QyXYxlUHOJrIj6o130_assertion evidence source_evidence_literature NP690528.RAVLHgQtnzm4u14PIgNypeITteG4p_QyXYxlUHOJrIj6o130_provenance.
- NP690528.RAVLHgQtnzm4u14PIgNypeITteG4p_QyXYxlUHOJrIj6o130_assertion SIO_000772 18757851 NP690528.RAVLHgQtnzm4u14PIgNypeITteG4p_QyXYxlUHOJrIj6o130_provenance.
- NP690528.RAVLHgQtnzm4u14PIgNypeITteG4p_QyXYxlUHOJrIj6o130_assertion wasDerivedFrom befree-2016 NP690528.RAVLHgQtnzm4u14PIgNypeITteG4p_QyXYxlUHOJrIj6o130_provenance.
- NP690528.RAVLHgQtnzm4u14PIgNypeITteG4p_QyXYxlUHOJrIj6o130_assertion wasGeneratedBy ECO_0000203 NP690528.RAVLHgQtnzm4u14PIgNypeITteG4p_QyXYxlUHOJrIj6o130_provenance.
- befree-2016 importedOn "2016-02-19" NP690528.RAVLHgQtnzm4u14PIgNypeITteG4p_QyXYxlUHOJrIj6o130_provenance.