Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_provenance.
- NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_assertion description "[Although we initially focused on the mutation in POLG2, the mutation in OPA1 is more likely to explain the late-onset PEO and multisystem disorder in this patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_provenance.
- NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_assertion evidence source_evidence_literature NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_provenance.
- NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_assertion SIO_000772 18195150 NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_provenance.
- NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_assertion wasDerivedFrom befree-20150227 NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_provenance.
- NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_assertion wasGeneratedBy ECO_0000203 NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_provenance.