Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP867202.RAgBbT6b0p5ZtUZIDIwAkpfp7Vl4sIUbQ8KUgjf7vu79Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP867202.RAgBbT6b0p5ZtUZIDIwAkpfp7Vl4sIUbQ8KUgjf7vu79Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867202.RAgBbT6b0p5ZtUZIDIwAkpfp7Vl4sIUbQ8KUgjf7vu79Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867202.RAgBbT6b0p5ZtUZIDIwAkpfp7Vl4sIUbQ8KUgjf7vu79Y130_provenance.
- NP867202.RAgBbT6b0p5ZtUZIDIwAkpfp7Vl4sIUbQ8KUgjf7vu79Y130_assertion description "[Mutations in the gene mitofusin 2 (MFN2) cause the axonal subtype CMT2A, which has also been shown to be associated with optic atrophy, clinical signs of first motor neuron involvement, and early onset stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867202.RAgBbT6b0p5ZtUZIDIwAkpfp7Vl4sIUbQ8KUgjf7vu79Y130_provenance.
- NP867202.RAgBbT6b0p5ZtUZIDIwAkpfp7Vl4sIUbQ8KUgjf7vu79Y130_assertion evidence source_evidence_literature NP867202.RAgBbT6b0p5ZtUZIDIwAkpfp7Vl4sIUbQ8KUgjf7vu79Y130_provenance.
- NP867202.RAgBbT6b0p5ZtUZIDIwAkpfp7Vl4sIUbQ8KUgjf7vu79Y130_assertion SIO_000772 21258814 NP867202.RAgBbT6b0p5ZtUZIDIwAkpfp7Vl4sIUbQ8KUgjf7vu79Y130_provenance.
- NP867202.RAgBbT6b0p5ZtUZIDIwAkpfp7Vl4sIUbQ8KUgjf7vu79Y130_assertion wasDerivedFrom befree-2016 NP867202.RAgBbT6b0p5ZtUZIDIwAkpfp7Vl4sIUbQ8KUgjf7vu79Y130_provenance.
- NP867202.RAgBbT6b0p5ZtUZIDIwAkpfp7Vl4sIUbQ8KUgjf7vu79Y130_assertion wasGeneratedBy ECO_0000203 NP867202.RAgBbT6b0p5ZtUZIDIwAkpfp7Vl4sIUbQ8KUgjf7vu79Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP867202.RAgBbT6b0p5ZtUZIDIwAkpfp7Vl4sIUbQ8KUgjf7vu79Y130_provenance.