Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP593319.RALpOjPHuJWRSac5LcQe_i64E1ALBy6-P0rSV7ksi0Rnc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP593319.RALpOjPHuJWRSac5LcQe_i64E1ALBy6-P0rSV7ksi0Rnc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP593319.RALpOjPHuJWRSac5LcQe_i64E1ALBy6-P0rSV7ksi0Rnc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP593319.RALpOjPHuJWRSac5LcQe_i64E1ALBy6-P0rSV7ksi0Rnc130_provenance.
- NP593319.RALpOjPHuJWRSac5LcQe_i64E1ALBy6-P0rSV7ksi0Rnc130_assertion description "[To compare the distributions of mutations/polymorphisms in genes affecting hemostasis (factor V Leiden - FVL, FV H1298R-FVR2, FII 20210A, b-Fib 455G>A, FXIII V34L, PAI-1 4G, HPA-1b) or homocysteine metabolism (MTHFR C677T, MTHFR A1298C) among 90 children with arterial ischemic stroke (AIS) and 103 controls, and to associate the carriage of these mutations/polymorphisms with their corresponding proteins in children with AIS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593319.RALpOjPHuJWRSac5LcQe_i64E1ALBy6-P0rSV7ksi0Rnc130_provenance.
- NP593319.RALpOjPHuJWRSac5LcQe_i64E1ALBy6-P0rSV7ksi0Rnc130_assertion evidence source_evidence_literature NP593319.RALpOjPHuJWRSac5LcQe_i64E1ALBy6-P0rSV7ksi0Rnc130_provenance.
- NP593319.RALpOjPHuJWRSac5LcQe_i64E1ALBy6-P0rSV7ksi0Rnc130_assertion SIO_000772 16567932 NP593319.RALpOjPHuJWRSac5LcQe_i64E1ALBy6-P0rSV7ksi0Rnc130_provenance.
- NP593319.RALpOjPHuJWRSac5LcQe_i64E1ALBy6-P0rSV7ksi0Rnc130_assertion wasDerivedFrom befree-20140225 NP593319.RALpOjPHuJWRSac5LcQe_i64E1ALBy6-P0rSV7ksi0Rnc130_provenance.
- NP593319.RALpOjPHuJWRSac5LcQe_i64E1ALBy6-P0rSV7ksi0Rnc130_assertion wasGeneratedBy ECO_0000203 NP593319.RALpOjPHuJWRSac5LcQe_i64E1ALBy6-P0rSV7ksi0Rnc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP593319.RALpOjPHuJWRSac5LcQe_i64E1ALBy6-P0rSV7ksi0Rnc130_provenance.