Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP598524.RAxRDpmWOmDmTYbl_ZXJPKgcs6yGD7HiPQFJ2NlJr7i50130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP598524.RAxRDpmWOmDmTYbl_ZXJPKgcs6yGD7HiPQFJ2NlJr7i50130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP598524.RAxRDpmWOmDmTYbl_ZXJPKgcs6yGD7HiPQFJ2NlJr7i50130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP598524.RAxRDpmWOmDmTYbl_ZXJPKgcs6yGD7HiPQFJ2NlJr7i50130_provenance.
- NP598524.RAxRDpmWOmDmTYbl_ZXJPKgcs6yGD7HiPQFJ2NlJr7i50130_assertion description "[To test this hypothesis, we performed case-control analyses on all DNA polymorphic variation identified in a resequencing study of six candidate DCM genes (CSRP3, LDB3, MYH7, SCN5A, TCAP, and TNNT2) conducted in 289 unrelated white probands with DCM of unknown cause and 188 unrelated white controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598524.RAxRDpmWOmDmTYbl_ZXJPKgcs6yGD7HiPQFJ2NlJr7i50130_provenance.
- NP598524.RAxRDpmWOmDmTYbl_ZXJPKgcs6yGD7HiPQFJ2NlJr7i50130_assertion evidence source_evidence_literature NP598524.RAxRDpmWOmDmTYbl_ZXJPKgcs6yGD7HiPQFJ2NlJr7i50130_provenance.
- NP598524.RAxRDpmWOmDmTYbl_ZXJPKgcs6yGD7HiPQFJ2NlJr7i50130_assertion SIO_000772 20201937 NP598524.RAxRDpmWOmDmTYbl_ZXJPKgcs6yGD7HiPQFJ2NlJr7i50130_provenance.
- NP598524.RAxRDpmWOmDmTYbl_ZXJPKgcs6yGD7HiPQFJ2NlJr7i50130_assertion wasDerivedFrom befree-20140225 NP598524.RAxRDpmWOmDmTYbl_ZXJPKgcs6yGD7HiPQFJ2NlJr7i50130_provenance.
- NP598524.RAxRDpmWOmDmTYbl_ZXJPKgcs6yGD7HiPQFJ2NlJr7i50130_assertion wasGeneratedBy ECO_0000203 NP598524.RAxRDpmWOmDmTYbl_ZXJPKgcs6yGD7HiPQFJ2NlJr7i50130_provenance.
- befree-20140225 importedOn "2014-02-25" NP598524.RAxRDpmWOmDmTYbl_ZXJPKgcs6yGD7HiPQFJ2NlJr7i50130_provenance.