Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP216660.RAPRzX26UhWrNDFRkXuLdUeFbyOjvpjKFvSP7W7_KaBsU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP216660.RAPRzX26UhWrNDFRkXuLdUeFbyOjvpjKFvSP7W7_KaBsU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP216660.RAPRzX26UhWrNDFRkXuLdUeFbyOjvpjKFvSP7W7_KaBsU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP216660.RAPRzX26UhWrNDFRkXuLdUeFbyOjvpjKFvSP7W7_KaBsU130_provenance.
- NP216660.RAPRzX26UhWrNDFRkXuLdUeFbyOjvpjKFvSP7W7_KaBsU130_assertion description "[Alpers syndrome patients with tissue depletion of mtDNA had at least one allele with mutation in the catalytic domain of POLG1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216660.RAPRzX26UhWrNDFRkXuLdUeFbyOjvpjKFvSP7W7_KaBsU130_provenance.
- NP216660.RAPRzX26UhWrNDFRkXuLdUeFbyOjvpjKFvSP7W7_KaBsU130_assertion evidence source_evidence_literature NP216660.RAPRzX26UhWrNDFRkXuLdUeFbyOjvpjKFvSP7W7_KaBsU130_provenance.
- NP216660.RAPRzX26UhWrNDFRkXuLdUeFbyOjvpjKFvSP7W7_KaBsU130_assertion SIO_000772 18487244 NP216660.RAPRzX26UhWrNDFRkXuLdUeFbyOjvpjKFvSP7W7_KaBsU130_provenance.
- NP216660.RAPRzX26UhWrNDFRkXuLdUeFbyOjvpjKFvSP7W7_KaBsU130_assertion wasDerivedFrom lhgdn-20090331 NP216660.RAPRzX26UhWrNDFRkXuLdUeFbyOjvpjKFvSP7W7_KaBsU130_provenance.
- NP216660.RAPRzX26UhWrNDFRkXuLdUeFbyOjvpjKFvSP7W7_KaBsU130_assertion wasGeneratedBy ECO_0000203 NP216660.RAPRzX26UhWrNDFRkXuLdUeFbyOjvpjKFvSP7W7_KaBsU130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP216660.RAPRzX26UhWrNDFRkXuLdUeFbyOjvpjKFvSP7W7_KaBsU130_provenance.