Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1217421.RA2gaU4cPdHJ_V7cxxghhf5rA6OcvBYLP976B6HmkjWwQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1217421.RA2gaU4cPdHJ_V7cxxghhf5rA6OcvBYLP976B6HmkjWwQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1217421.RA2gaU4cPdHJ_V7cxxghhf5rA6OcvBYLP976B6HmkjWwQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1217421.RA2gaU4cPdHJ_V7cxxghhf5rA6OcvBYLP976B6HmkjWwQ130_provenance.
- NP1217421.RA2gaU4cPdHJ_V7cxxghhf5rA6OcvBYLP976B6HmkjWwQ130_assertion description "[Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1217421.RA2gaU4cPdHJ_V7cxxghhf5rA6OcvBYLP976B6HmkjWwQ130_provenance.
- NP1217421.RA2gaU4cPdHJ_V7cxxghhf5rA6OcvBYLP976B6HmkjWwQ130_assertion evidence source_evidence_literature NP1217421.RA2gaU4cPdHJ_V7cxxghhf5rA6OcvBYLP976B6HmkjWwQ130_provenance.
- NP1217421.RA2gaU4cPdHJ_V7cxxghhf5rA6OcvBYLP976B6HmkjWwQ130_assertion SIO_000772 25193783 NP1217421.RA2gaU4cPdHJ_V7cxxghhf5rA6OcvBYLP976B6HmkjWwQ130_provenance.
- NP1217421.RA2gaU4cPdHJ_V7cxxghhf5rA6OcvBYLP976B6HmkjWwQ130_assertion wasDerivedFrom befree-2016 NP1217421.RA2gaU4cPdHJ_V7cxxghhf5rA6OcvBYLP976B6HmkjWwQ130_provenance.
- NP1217421.RA2gaU4cPdHJ_V7cxxghhf5rA6OcvBYLP976B6HmkjWwQ130_assertion wasGeneratedBy ECO_0000203 NP1217421.RA2gaU4cPdHJ_V7cxxghhf5rA6OcvBYLP976B6HmkjWwQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1217421.RA2gaU4cPdHJ_V7cxxghhf5rA6OcvBYLP976B6HmkjWwQ130_provenance.