Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP685035.RAIqqKOsX2NxR0gRHfZ6_SZ0qNRGnQgIUT3bPsdJCickY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP685035.RAIqqKOsX2NxR0gRHfZ6_SZ0qNRGnQgIUT3bPsdJCickY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP685035.RAIqqKOsX2NxR0gRHfZ6_SZ0qNRGnQgIUT3bPsdJCickY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP685035.RAIqqKOsX2NxR0gRHfZ6_SZ0qNRGnQgIUT3bPsdJCickY130_provenance.
- NP685035.RAIqqKOsX2NxR0gRHfZ6_SZ0qNRGnQgIUT3bPsdJCickY130_assertion wasGeneratedBy ECO_0000203 NP685035.RAIqqKOsX2NxR0gRHfZ6_SZ0qNRGnQgIUT3bPsdJCickY130_provenance.
- NP685035.RAIqqKOsX2NxR0gRHfZ6_SZ0qNRGnQgIUT3bPsdJCickY130_assertion wasDerivedFrom befree-20140225 NP685035.RAIqqKOsX2NxR0gRHfZ6_SZ0qNRGnQgIUT3bPsdJCickY130_provenance.
- NP685035.RAIqqKOsX2NxR0gRHfZ6_SZ0qNRGnQgIUT3bPsdJCickY130_assertion SIO_000772 19195941 NP685035.RAIqqKOsX2NxR0gRHfZ6_SZ0qNRGnQgIUT3bPsdJCickY130_provenance.
- NP685035.RAIqqKOsX2NxR0gRHfZ6_SZ0qNRGnQgIUT3bPsdJCickY130_assertion evidence source_evidence_literature NP685035.RAIqqKOsX2NxR0gRHfZ6_SZ0qNRGnQgIUT3bPsdJCickY130_provenance.
- NP685035.RAIqqKOsX2NxR0gRHfZ6_SZ0qNRGnQgIUT3bPsdJCickY130_assertion description "[Our data further expand the spectrum of POLG1 gene mutations and the unique phenotype reported (late onset isolated liver disease without lactic acidosis) increase the variability of clinical presentations associated with mutations in this gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP685035.RAIqqKOsX2NxR0gRHfZ6_SZ0qNRGnQgIUT3bPsdJCickY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP685035.RAIqqKOsX2NxR0gRHfZ6_SZ0qNRGnQgIUT3bPsdJCickY130_provenance.