Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP297006.RAWN6FPzs2VzH519d0c4evOZLbIBeTyGhGd9lAEP1BqZE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP297006.RAWN6FPzs2VzH519d0c4evOZLbIBeTyGhGd9lAEP1BqZE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP297006.RAWN6FPzs2VzH519d0c4evOZLbIBeTyGhGd9lAEP1BqZE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP297006.RAWN6FPzs2VzH519d0c4evOZLbIBeTyGhGd9lAEP1BqZE130_provenance.
- NP297006.RAWN6FPzs2VzH519d0c4evOZLbIBeTyGhGd9lAEP1BqZE130_assertion description "[More importantly, prevalence of the LRP1 2080D allele was not increased in the group of patients with high FVIII:C and VTE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297006.RAWN6FPzs2VzH519d0c4evOZLbIBeTyGhGd9lAEP1BqZE130_provenance.
- NP297006.RAWN6FPzs2VzH519d0c4evOZLbIBeTyGhGd9lAEP1BqZE130_assertion evidence source_evidence_literature NP297006.RAWN6FPzs2VzH519d0c4evOZLbIBeTyGhGd9lAEP1BqZE130_provenance.
- NP297006.RAWN6FPzs2VzH519d0c4evOZLbIBeTyGhGd9lAEP1BqZE130_assertion SIO_000772 16175004 NP297006.RAWN6FPzs2VzH519d0c4evOZLbIBeTyGhGd9lAEP1BqZE130_provenance.
- NP297006.RAWN6FPzs2VzH519d0c4evOZLbIBeTyGhGd9lAEP1BqZE130_assertion wasDerivedFrom befree-20140225 NP297006.RAWN6FPzs2VzH519d0c4evOZLbIBeTyGhGd9lAEP1BqZE130_provenance.
- NP297006.RAWN6FPzs2VzH519d0c4evOZLbIBeTyGhGd9lAEP1BqZE130_assertion wasGeneratedBy ECO_0000203 NP297006.RAWN6FPzs2VzH519d0c4evOZLbIBeTyGhGd9lAEP1BqZE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP297006.RAWN6FPzs2VzH519d0c4evOZLbIBeTyGhGd9lAEP1BqZE130_provenance.