Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP720603.RA1wXWc0oDwMrjHTlTCSDQzg-SE-vXEFqFzgCiryFELwg130_assertion> ?p ?o ?g. }
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- NP720603.RA1wXWc0oDwMrjHTlTCSDQzg-SE-vXEFqFzgCiryFELwg130_assertion type Assertion NP720603.RA1wXWc0oDwMrjHTlTCSDQzg-SE-vXEFqFzgCiryFELwg130_head.
- NP720603.RA1wXWc0oDwMrjHTlTCSDQzg-SE-vXEFqFzgCiryFELwg130_assertion description "[Two of the most common clinical presentations, Leigh Syndrome and hypertrophic cardiomyopathy, have so far only been associated with mutations in SURF1 or SCO2 and COX15, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720603.RA1wXWc0oDwMrjHTlTCSDQzg-SE-vXEFqFzgCiryFELwg130_provenance.
- NP720603.RA1wXWc0oDwMrjHTlTCSDQzg-SE-vXEFqFzgCiryFELwg130_assertion evidence source_evidence_literature NP720603.RA1wXWc0oDwMrjHTlTCSDQzg-SE-vXEFqFzgCiryFELwg130_provenance.
- NP720603.RA1wXWc0oDwMrjHTlTCSDQzg-SE-vXEFqFzgCiryFELwg130_assertion SIO_000772 12928484 NP720603.RA1wXWc0oDwMrjHTlTCSDQzg-SE-vXEFqFzgCiryFELwg130_provenance.
- NP720603.RA1wXWc0oDwMrjHTlTCSDQzg-SE-vXEFqFzgCiryFELwg130_assertion wasDerivedFrom befree-20150227 NP720603.RA1wXWc0oDwMrjHTlTCSDQzg-SE-vXEFqFzgCiryFELwg130_provenance.
- NP720603.RA1wXWc0oDwMrjHTlTCSDQzg-SE-vXEFqFzgCiryFELwg130_assertion wasGeneratedBy ECO_0000203 NP720603.RA1wXWc0oDwMrjHTlTCSDQzg-SE-vXEFqFzgCiryFELwg130_provenance.