Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1215629.RAPcrYrz9k0O7aumwzPYpBqA7njFmd2vsq58-O1Bio6M0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1215629.RAPcrYrz9k0O7aumwzPYpBqA7njFmd2vsq58-O1Bio6M0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1215629.RAPcrYrz9k0O7aumwzPYpBqA7njFmd2vsq58-O1Bio6M0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1215629.RAPcrYrz9k0O7aumwzPYpBqA7njFmd2vsq58-O1Bio6M0130_provenance.
- NP1215629.RAPcrYrz9k0O7aumwzPYpBqA7njFmd2vsq58-O1Bio6M0130_assertion description "[Mutations in APOPT1, encoding a mitochondrial protein, cause cavitating leukoencephalopathy with cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1215629.RAPcrYrz9k0O7aumwzPYpBqA7njFmd2vsq58-O1Bio6M0130_provenance.
- NP1215629.RAPcrYrz9k0O7aumwzPYpBqA7njFmd2vsq58-O1Bio6M0130_assertion evidence source_evidence_literature NP1215629.RAPcrYrz9k0O7aumwzPYpBqA7njFmd2vsq58-O1Bio6M0130_provenance.
- NP1215629.RAPcrYrz9k0O7aumwzPYpBqA7njFmd2vsq58-O1Bio6M0130_assertion SIO_000772 25175347 NP1215629.RAPcrYrz9k0O7aumwzPYpBqA7njFmd2vsq58-O1Bio6M0130_provenance.
- NP1215629.RAPcrYrz9k0O7aumwzPYpBqA7njFmd2vsq58-O1Bio6M0130_assertion wasDerivedFrom befree-2016 NP1215629.RAPcrYrz9k0O7aumwzPYpBqA7njFmd2vsq58-O1Bio6M0130_provenance.
- NP1215629.RAPcrYrz9k0O7aumwzPYpBqA7njFmd2vsq58-O1Bio6M0130_assertion wasGeneratedBy ECO_0000203 NP1215629.RAPcrYrz9k0O7aumwzPYpBqA7njFmd2vsq58-O1Bio6M0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1215629.RAPcrYrz9k0O7aumwzPYpBqA7njFmd2vsq58-O1Bio6M0130_provenance.