Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP198123.RAvhHc-4LEhBUeHZt-uXIsQzDovX6TRCeo_eC2fKFOqzQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP198123.RAvhHc-4LEhBUeHZt-uXIsQzDovX6TRCeo_eC2fKFOqzQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP198123.RAvhHc-4LEhBUeHZt-uXIsQzDovX6TRCeo_eC2fKFOqzQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP198123.RAvhHc-4LEhBUeHZt-uXIsQzDovX6TRCeo_eC2fKFOqzQ130_provenance.
- NP198123.RAvhHc-4LEhBUeHZt-uXIsQzDovX6TRCeo_eC2fKFOqzQ130_assertion description "[Two siblings heterozygous for the mutations A460V and V572L/sibs had Nonaka myopathy (OMIM 605820).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198123.RAvhHc-4LEhBUeHZt-uXIsQzDovX6TRCeo_eC2fKFOqzQ130_provenance.
- NP198123.RAvhHc-4LEhBUeHZt-uXIsQzDovX6TRCeo_eC2fKFOqzQ130_assertion evidence source_evidence_literature NP198123.RAvhHc-4LEhBUeHZt-uXIsQzDovX6TRCeo_eC2fKFOqzQ130_provenance.
- NP198123.RAvhHc-4LEhBUeHZt-uXIsQzDovX6TRCeo_eC2fKFOqzQ130_assertion SIO_000772 11916006 NP198123.RAvhHc-4LEhBUeHZt-uXIsQzDovX6TRCeo_eC2fKFOqzQ130_provenance.
- NP198123.RAvhHc-4LEhBUeHZt-uXIsQzDovX6TRCeo_eC2fKFOqzQ130_assertion wasDerivedFrom lhgdn-20090331 NP198123.RAvhHc-4LEhBUeHZt-uXIsQzDovX6TRCeo_eC2fKFOqzQ130_provenance.
- NP198123.RAvhHc-4LEhBUeHZt-uXIsQzDovX6TRCeo_eC2fKFOqzQ130_assertion wasGeneratedBy ECO_0000203 NP198123.RAvhHc-4LEhBUeHZt-uXIsQzDovX6TRCeo_eC2fKFOqzQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP198123.RAvhHc-4LEhBUeHZt-uXIsQzDovX6TRCeo_eC2fKFOqzQ130_provenance.