Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP809380.RAtk0hTZNN4tbZM5sCZ0J66Dc0QRsCeLPQGG2ma19-kcs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP809380.RAtk0hTZNN4tbZM5sCZ0J66Dc0QRsCeLPQGG2ma19-kcs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP809380.RAtk0hTZNN4tbZM5sCZ0J66Dc0QRsCeLPQGG2ma19-kcs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP809380.RAtk0hTZNN4tbZM5sCZ0J66Dc0QRsCeLPQGG2ma19-kcs130_provenance.
- NP809380.RAtk0hTZNN4tbZM5sCZ0J66Dc0QRsCeLPQGG2ma19-kcs130_assertion description "[Mmutations in paraplegin, a putative mitochondrial metallopeptidase of the AAA family, cause an autosomal recessive form of hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809380.RAtk0hTZNN4tbZM5sCZ0J66Dc0QRsCeLPQGG2ma19-kcs130_provenance.
- NP809380.RAtk0hTZNN4tbZM5sCZ0J66Dc0QRsCeLPQGG2ma19-kcs130_assertion evidence source_evidence_literature NP809380.RAtk0hTZNN4tbZM5sCZ0J66Dc0QRsCeLPQGG2ma19-kcs130_provenance.
- NP809380.RAtk0hTZNN4tbZM5sCZ0J66Dc0QRsCeLPQGG2ma19-kcs130_assertion SIO_000772 14623864 NP809380.RAtk0hTZNN4tbZM5sCZ0J66Dc0QRsCeLPQGG2ma19-kcs130_provenance.
- NP809380.RAtk0hTZNN4tbZM5sCZ0J66Dc0QRsCeLPQGG2ma19-kcs130_assertion wasDerivedFrom befree-20140225 NP809380.RAtk0hTZNN4tbZM5sCZ0J66Dc0QRsCeLPQGG2ma19-kcs130_provenance.
- NP809380.RAtk0hTZNN4tbZM5sCZ0J66Dc0QRsCeLPQGG2ma19-kcs130_assertion wasGeneratedBy ECO_0000203 NP809380.RAtk0hTZNN4tbZM5sCZ0J66Dc0QRsCeLPQGG2ma19-kcs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP809380.RAtk0hTZNN4tbZM5sCZ0J66Dc0QRsCeLPQGG2ma19-kcs130_provenance.