Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP227475.RAWN9TxaAtxbcyai_R7s9sUI_9PbLhHquttvgkSAX1ihU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP227475.RAWN9TxaAtxbcyai_R7s9sUI_9PbLhHquttvgkSAX1ihU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP227475.RAWN9TxaAtxbcyai_R7s9sUI_9PbLhHquttvgkSAX1ihU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP227475.RAWN9TxaAtxbcyai_R7s9sUI_9PbLhHquttvgkSAX1ihU130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP227475.RAWN9TxaAtxbcyai_R7s9sUI_9PbLhHquttvgkSAX1ihU130_provenance.
- NP227475.RAWN9TxaAtxbcyai_R7s9sUI_9PbLhHquttvgkSAX1ihU130_assertion wasGeneratedBy ECO_0000203 NP227475.RAWN9TxaAtxbcyai_R7s9sUI_9PbLhHquttvgkSAX1ihU130_provenance.
- NP227475.RAWN9TxaAtxbcyai_R7s9sUI_9PbLhHquttvgkSAX1ihU130_assertion wasDerivedFrom lhgdn-20090331 NP227475.RAWN9TxaAtxbcyai_R7s9sUI_9PbLhHquttvgkSAX1ihU130_provenance.
- NP227475.RAWN9TxaAtxbcyai_R7s9sUI_9PbLhHquttvgkSAX1ihU130_assertion SIO_000772 17650440 NP227475.RAWN9TxaAtxbcyai_R7s9sUI_9PbLhHquttvgkSAX1ihU130_provenance.
- NP227475.RAWN9TxaAtxbcyai_R7s9sUI_9PbLhHquttvgkSAX1ihU130_assertion evidence source_evidence_literature NP227475.RAWN9TxaAtxbcyai_R7s9sUI_9PbLhHquttvgkSAX1ihU130_provenance.
- NP227475.RAWN9TxaAtxbcyai_R7s9sUI_9PbLhHquttvgkSAX1ihU130_assertion description "[heterozygous carriers of FVL who experience an episode of venous thromboembolism (VTE) have on average a 40% increased risk of recurrent VTE over non-carriers; risk is lower with heterozygosity of prothrombin G20210A mutation [review]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP227475.RAWN9TxaAtxbcyai_R7s9sUI_9PbLhHquttvgkSAX1ihU130_provenance.