Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP87825.RAbclEovErQgCc48QwfVFjbV0G0gLP0Tcn2rmFsVW3EE8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP87825.RAbclEovErQgCc48QwfVFjbV0G0gLP0Tcn2rmFsVW3EE8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP87825.RAbclEovErQgCc48QwfVFjbV0G0gLP0Tcn2rmFsVW3EE8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP87825.RAbclEovErQgCc48QwfVFjbV0G0gLP0Tcn2rmFsVW3EE8130_provenance.
- NP87825.RAbclEovErQgCc48QwfVFjbV0G0gLP0Tcn2rmFsVW3EE8130_assertion description "[Association of common genetic variations and idiopathic venous thromboembolism. Results from EDITh, a hospital-based case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87825.RAbclEovErQgCc48QwfVFjbV0G0gLP0Tcn2rmFsVW3EE8130_provenance.
- NP87825.RAbclEovErQgCc48QwfVFjbV0G0gLP0Tcn2rmFsVW3EE8130_assertion evidence source_evidence_literature NP87825.RAbclEovErQgCc48QwfVFjbV0G0gLP0Tcn2rmFsVW3EE8130_provenance.
- NP87825.RAbclEovErQgCc48QwfVFjbV0G0gLP0Tcn2rmFsVW3EE8130_assertion SIO_000772 20352152 NP87825.RAbclEovErQgCc48QwfVFjbV0G0gLP0Tcn2rmFsVW3EE8130_provenance.
- NP87825.RAbclEovErQgCc48QwfVFjbV0G0gLP0Tcn2rmFsVW3EE8130_assertion wasDerivedFrom gad-20130706 NP87825.RAbclEovErQgCc48QwfVFjbV0G0gLP0Tcn2rmFsVW3EE8130_provenance.
- NP87825.RAbclEovErQgCc48QwfVFjbV0G0gLP0Tcn2rmFsVW3EE8130_assertion wasGeneratedBy ECO_0000203 NP87825.RAbclEovErQgCc48QwfVFjbV0G0gLP0Tcn2rmFsVW3EE8130_provenance.
- gad-20130706 importedOn "2013-07-06" NP87825.RAbclEovErQgCc48QwfVFjbV0G0gLP0Tcn2rmFsVW3EE8130_provenance.