Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_provenance.
- NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_assertion description "[Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_provenance.
- NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_assertion evidence source_evidence_literature NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_provenance.
- NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_assertion SIO_000772 10749987 NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_provenance.
- NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_assertion wasDerivedFrom befree-2016 NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_provenance.
- NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_assertion wasGeneratedBy ECO_0000203 NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_provenance.
- befree-2016 importedOn "2016-02-19" NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_provenance.