Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP237797.RAf_gp907aPeKlcyj6nuJYcx88VjLhgY1Mv1TWwHD9HA4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP237797.RAf_gp907aPeKlcyj6nuJYcx88VjLhgY1Mv1TWwHD9HA4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP237797.RAf_gp907aPeKlcyj6nuJYcx88VjLhgY1Mv1TWwHD9HA4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP237797.RAf_gp907aPeKlcyj6nuJYcx88VjLhgY1Mv1TWwHD9HA4130_provenance.
- NP237797.RAf_gp907aPeKlcyj6nuJYcx88VjLhgY1Mv1TWwHD9HA4130_assertion description "[Second, because multiple regulatory factors affect SHBG levels and residual confounding may remain, we determined six single-nucleotide polymorphisms (SNPs) in the SHBG gene and assessed the risk of venous thrombosis in a different case-control study, the Leiden Thrombophilia Study (LETS) (20 patients; 74 controls), and in the MEGA study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237797.RAf_gp907aPeKlcyj6nuJYcx88VjLhgY1Mv1TWwHD9HA4130_provenance.
- NP237797.RAf_gp907aPeKlcyj6nuJYcx88VjLhgY1Mv1TWwHD9HA4130_assertion evidence source_evidence_literature NP237797.RAf_gp907aPeKlcyj6nuJYcx88VjLhgY1Mv1TWwHD9HA4130_provenance.
- NP237797.RAf_gp907aPeKlcyj6nuJYcx88VjLhgY1Mv1TWwHD9HA4130_assertion SIO_000772 22882730 NP237797.RAf_gp907aPeKlcyj6nuJYcx88VjLhgY1Mv1TWwHD9HA4130_provenance.
- NP237797.RAf_gp907aPeKlcyj6nuJYcx88VjLhgY1Mv1TWwHD9HA4130_assertion wasDerivedFrom befree-20140225 NP237797.RAf_gp907aPeKlcyj6nuJYcx88VjLhgY1Mv1TWwHD9HA4130_provenance.
- NP237797.RAf_gp907aPeKlcyj6nuJYcx88VjLhgY1Mv1TWwHD9HA4130_assertion wasGeneratedBy ECO_0000203 NP237797.RAf_gp907aPeKlcyj6nuJYcx88VjLhgY1Mv1TWwHD9HA4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP237797.RAf_gp907aPeKlcyj6nuJYcx88VjLhgY1Mv1TWwHD9HA4130_provenance.