Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP624448.RAcJEDECX60PkSUQhfVPFo33rMFKbe7JJRoOoJtP9rjFA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP624448.RAcJEDECX60PkSUQhfVPFo33rMFKbe7JJRoOoJtP9rjFA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP624448.RAcJEDECX60PkSUQhfVPFo33rMFKbe7JJRoOoJtP9rjFA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP624448.RAcJEDECX60PkSUQhfVPFo33rMFKbe7JJRoOoJtP9rjFA130_provenance.
- NP624448.RAcJEDECX60PkSUQhfVPFo33rMFKbe7JJRoOoJtP9rjFA130_assertion description "[All patients underwent comprehensive tests for coagulation disorders including determinations of protein C, protein S, lupus anticoagulants, prothrombin gene mutation (G20210A), resistance to activated protein C (APCR), and were screened for vascular disease risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP624448.RAcJEDECX60PkSUQhfVPFo33rMFKbe7JJRoOoJtP9rjFA130_provenance.
- NP624448.RAcJEDECX60PkSUQhfVPFo33rMFKbe7JJRoOoJtP9rjFA130_assertion evidence source_evidence_literature NP624448.RAcJEDECX60PkSUQhfVPFo33rMFKbe7JJRoOoJtP9rjFA130_provenance.
- NP624448.RAcJEDECX60PkSUQhfVPFo33rMFKbe7JJRoOoJtP9rjFA130_assertion SIO_000772 11456253 NP624448.RAcJEDECX60PkSUQhfVPFo33rMFKbe7JJRoOoJtP9rjFA130_provenance.
- NP624448.RAcJEDECX60PkSUQhfVPFo33rMFKbe7JJRoOoJtP9rjFA130_assertion wasDerivedFrom befree-20140225 NP624448.RAcJEDECX60PkSUQhfVPFo33rMFKbe7JJRoOoJtP9rjFA130_provenance.
- NP624448.RAcJEDECX60PkSUQhfVPFo33rMFKbe7JJRoOoJtP9rjFA130_assertion wasGeneratedBy ECO_0000203 NP624448.RAcJEDECX60PkSUQhfVPFo33rMFKbe7JJRoOoJtP9rjFA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP624448.RAcJEDECX60PkSUQhfVPFo33rMFKbe7JJRoOoJtP9rjFA130_provenance.