Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP699230.RAcZqpdxzNV8gSZxU1Tc2CqQJlWGw58aQfeVUcGol6R20130_assertion> ?p ?o ?g. }
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- NP699230.RAcZqpdxzNV8gSZxU1Tc2CqQJlWGw58aQfeVUcGol6R20130_assertion type Assertion NP699230.RAcZqpdxzNV8gSZxU1Tc2CqQJlWGw58aQfeVUcGol6R20130_head.
- NP699230.RAcZqpdxzNV8gSZxU1Tc2CqQJlWGw58aQfeVUcGol6R20130_assertion wasGeneratedBy ECO_0000203 NP699230.RAcZqpdxzNV8gSZxU1Tc2CqQJlWGw58aQfeVUcGol6R20130_provenance.
- NP699230.RAcZqpdxzNV8gSZxU1Tc2CqQJlWGw58aQfeVUcGol6R20130_assertion wasDerivedFrom befree-20140225 NP699230.RAcZqpdxzNV8gSZxU1Tc2CqQJlWGw58aQfeVUcGol6R20130_provenance.
- NP699230.RAcZqpdxzNV8gSZxU1Tc2CqQJlWGw58aQfeVUcGol6R20130_assertion SIO_000772 21907713 NP699230.RAcZqpdxzNV8gSZxU1Tc2CqQJlWGw58aQfeVUcGol6R20130_provenance.
- NP699230.RAcZqpdxzNV8gSZxU1Tc2CqQJlWGw58aQfeVUcGol6R20130_assertion evidence source_evidence_literature NP699230.RAcZqpdxzNV8gSZxU1Tc2CqQJlWGw58aQfeVUcGol6R20130_provenance.
- NP699230.RAcZqpdxzNV8gSZxU1Tc2CqQJlWGw58aQfeVUcGol6R20130_assertion description "[Mutations in HCCS on the C-terminal side of the CP motifs, known to cause disease states in humans (microphthalmia with linear skin defects) abolished or drastically attenuated holocytochrome c production.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699230.RAcZqpdxzNV8gSZxU1Tc2CqQJlWGw58aQfeVUcGol6R20130_provenance.