Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP699230.RAcZqpdxzNV8gSZxU1Tc2CqQJlWGw58aQfeVUcGol6R20130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP699230.RAcZqpdxzNV8gSZxU1Tc2CqQJlWGw58aQfeVUcGol6R20130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP699230.RAcZqpdxzNV8gSZxU1Tc2CqQJlWGw58aQfeVUcGol6R20130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP699230.RAcZqpdxzNV8gSZxU1Tc2CqQJlWGw58aQfeVUcGol6R20130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP699230.RAcZqpdxzNV8gSZxU1Tc2CqQJlWGw58aQfeVUcGol6R20130_provenance.