Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP940051.RAIsAPK8yFz5iwZCaNB_41Cb1WBfotnl2xpnxeHTsOzX8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP940051.RAIsAPK8yFz5iwZCaNB_41Cb1WBfotnl2xpnxeHTsOzX8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP940051.RAIsAPK8yFz5iwZCaNB_41Cb1WBfotnl2xpnxeHTsOzX8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP940051.RAIsAPK8yFz5iwZCaNB_41Cb1WBfotnl2xpnxeHTsOzX8130_provenance.
- NP940051.RAIsAPK8yFz5iwZCaNB_41Cb1WBfotnl2xpnxeHTsOzX8130_assertion description "[The present investigation provides evidence for an association of the P2RY12 haplotype H2 with lower risk of DVT/PE; however these findings require replication in other well-designed studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP940051.RAIsAPK8yFz5iwZCaNB_41Cb1WBfotnl2xpnxeHTsOzX8130_provenance.
- NP940051.RAIsAPK8yFz5iwZCaNB_41Cb1WBfotnl2xpnxeHTsOzX8130_assertion evidence source_evidence_literature NP940051.RAIsAPK8yFz5iwZCaNB_41Cb1WBfotnl2xpnxeHTsOzX8130_provenance.
- NP940051.RAIsAPK8yFz5iwZCaNB_41Cb1WBfotnl2xpnxeHTsOzX8130_assertion SIO_000772 17707382 NP940051.RAIsAPK8yFz5iwZCaNB_41Cb1WBfotnl2xpnxeHTsOzX8130_provenance.
- NP940051.RAIsAPK8yFz5iwZCaNB_41Cb1WBfotnl2xpnxeHTsOzX8130_assertion wasDerivedFrom befree-20150227 NP940051.RAIsAPK8yFz5iwZCaNB_41Cb1WBfotnl2xpnxeHTsOzX8130_provenance.
- NP940051.RAIsAPK8yFz5iwZCaNB_41Cb1WBfotnl2xpnxeHTsOzX8130_assertion wasGeneratedBy ECO_0000203 NP940051.RAIsAPK8yFz5iwZCaNB_41Cb1WBfotnl2xpnxeHTsOzX8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP940051.RAIsAPK8yFz5iwZCaNB_41Cb1WBfotnl2xpnxeHTsOzX8130_provenance.