Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_assertion> ?p ?o ?g. }
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- NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_assertion type Assertion NP280134.RAi5uHiA8LxSCdET8855bLGTFc311EJID2Qr1yp0SLb5g130_head.
- 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.