Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP592132.RAUcn4AqRnYX6jo4ai3WL9anzxQZlpLjAmYrtP_UposAU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP592132.RAUcn4AqRnYX6jo4ai3WL9anzxQZlpLjAmYrtP_UposAU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP592132.RAUcn4AqRnYX6jo4ai3WL9anzxQZlpLjAmYrtP_UposAU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP592132.RAUcn4AqRnYX6jo4ai3WL9anzxQZlpLjAmYrtP_UposAU130_provenance.
- NP592132.RAUcn4AqRnYX6jo4ai3WL9anzxQZlpLjAmYrtP_UposAU130_assertion description "[A novel mutation in the human complex I NDUFS7 subunit associated with Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592132.RAUcn4AqRnYX6jo4ai3WL9anzxQZlpLjAmYrtP_UposAU130_provenance.
- NP592132.RAUcn4AqRnYX6jo4ai3WL9anzxQZlpLjAmYrtP_UposAU130_assertion evidence source_evidence_literature NP592132.RAUcn4AqRnYX6jo4ai3WL9anzxQZlpLjAmYrtP_UposAU130_provenance.
- NP592132.RAUcn4AqRnYX6jo4ai3WL9anzxQZlpLjAmYrtP_UposAU130_assertion SIO_000772 17275378 NP592132.RAUcn4AqRnYX6jo4ai3WL9anzxQZlpLjAmYrtP_UposAU130_provenance.
- NP592132.RAUcn4AqRnYX6jo4ai3WL9anzxQZlpLjAmYrtP_UposAU130_assertion wasDerivedFrom befree-2016 NP592132.RAUcn4AqRnYX6jo4ai3WL9anzxQZlpLjAmYrtP_UposAU130_provenance.
- NP592132.RAUcn4AqRnYX6jo4ai3WL9anzxQZlpLjAmYrtP_UposAU130_assertion wasGeneratedBy ECO_0000203 NP592132.RAUcn4AqRnYX6jo4ai3WL9anzxQZlpLjAmYrtP_UposAU130_provenance.
- befree-2016 importedOn "2016-02-19" NP592132.RAUcn4AqRnYX6jo4ai3WL9anzxQZlpLjAmYrtP_UposAU130_provenance.