Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_provenance.
- NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_assertion wasGeneratedBy ECO_0000203 NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_provenance.
- NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_assertion wasDerivedFrom lhgdn-20090331 NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_provenance.
- NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_assertion SIO_000772 15235026 NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_provenance.
- NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_assertion evidence source_evidence_literature NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_provenance.
- NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_assertion description "[A patient with typical clinical and neuroradiological features of Leigh syndrome and cytochrome oxidase deficiency was found to have a mutation in the COX15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199837.RAOv6zKJFJA1-rD9VVWLSNsF-qhAgtoe3bFbr0CyzQH1g130_provenance.