Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP572876.RABokDKZTllcBd0Pvf9Ir7hwgndtckJN5UwW3G8E8oHmE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP572876.RABokDKZTllcBd0Pvf9Ir7hwgndtckJN5UwW3G8E8oHmE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP572876.RABokDKZTllcBd0Pvf9Ir7hwgndtckJN5UwW3G8E8oHmE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP572876.RABokDKZTllcBd0Pvf9Ir7hwgndtckJN5UwW3G8E8oHmE130_provenance.
- NP572876.RABokDKZTllcBd0Pvf9Ir7hwgndtckJN5UwW3G8E8oHmE130_assertion description "[We suggest that specific point mutations in the CO1 and CO2 genes cause the CO defect in AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP572876.RABokDKZTllcBd0Pvf9Ir7hwgndtckJN5UwW3G8E8oHmE130_provenance.
- NP572876.RABokDKZTllcBd0Pvf9Ir7hwgndtckJN5UwW3G8E8oHmE130_assertion evidence source_evidence_literature NP572876.RABokDKZTllcBd0Pvf9Ir7hwgndtckJN5UwW3G8E8oHmE130_provenance.
- NP572876.RABokDKZTllcBd0Pvf9Ir7hwgndtckJN5UwW3G8E8oHmE130_assertion SIO_000772 9114023 NP572876.RABokDKZTllcBd0Pvf9Ir7hwgndtckJN5UwW3G8E8oHmE130_provenance.
- NP572876.RABokDKZTllcBd0Pvf9Ir7hwgndtckJN5UwW3G8E8oHmE130_assertion wasDerivedFrom befree-20150227 NP572876.RABokDKZTllcBd0Pvf9Ir7hwgndtckJN5UwW3G8E8oHmE130_provenance.
- NP572876.RABokDKZTllcBd0Pvf9Ir7hwgndtckJN5UwW3G8E8oHmE130_assertion wasGeneratedBy ECO_0000203 NP572876.RABokDKZTllcBd0Pvf9Ir7hwgndtckJN5UwW3G8E8oHmE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP572876.RABokDKZTllcBd0Pvf9Ir7hwgndtckJN5UwW3G8E8oHmE130_provenance.