Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP84321.RAMMKYowuU9rMfv_Pe3XyvgNAHR1NbMgGtMwqW4jjTqoM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP84321.RAMMKYowuU9rMfv_Pe3XyvgNAHR1NbMgGtMwqW4jjTqoM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP84321.RAMMKYowuU9rMfv_Pe3XyvgNAHR1NbMgGtMwqW4jjTqoM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP84321.RAMMKYowuU9rMfv_Pe3XyvgNAHR1NbMgGtMwqW4jjTqoM130_provenance.
- NP84321.RAMMKYowuU9rMfv_Pe3XyvgNAHR1NbMgGtMwqW4jjTqoM130_assertion description "[The factor V G1691A mutation is a risk for porencephaly: A case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP84321.RAMMKYowuU9rMfv_Pe3XyvgNAHR1NbMgGtMwqW4jjTqoM130_provenance.
- NP84321.RAMMKYowuU9rMfv_Pe3XyvgNAHR1NbMgGtMwqW4jjTqoM130_assertion evidence source_evidence_literature NP84321.RAMMKYowuU9rMfv_Pe3XyvgNAHR1NbMgGtMwqW4jjTqoM130_provenance.
- NP84321.RAMMKYowuU9rMfv_Pe3XyvgNAHR1NbMgGtMwqW4jjTqoM130_assertion SIO_000772 15293282 NP84321.RAMMKYowuU9rMfv_Pe3XyvgNAHR1NbMgGtMwqW4jjTqoM130_provenance.
- NP84321.RAMMKYowuU9rMfv_Pe3XyvgNAHR1NbMgGtMwqW4jjTqoM130_assertion wasDerivedFrom gad-20130706 NP84321.RAMMKYowuU9rMfv_Pe3XyvgNAHR1NbMgGtMwqW4jjTqoM130_provenance.
- NP84321.RAMMKYowuU9rMfv_Pe3XyvgNAHR1NbMgGtMwqW4jjTqoM130_assertion wasGeneratedBy ECO_0000203 NP84321.RAMMKYowuU9rMfv_Pe3XyvgNAHR1NbMgGtMwqW4jjTqoM130_provenance.
- gad-20130706 importedOn "2013-07-06" NP84321.RAMMKYowuU9rMfv_Pe3XyvgNAHR1NbMgGtMwqW4jjTqoM130_provenance.