Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP832479.RAYGLKGBFtMJVV_M8YqRRTQnQrY5baLYHL4tmn_67GcMU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP832479.RAYGLKGBFtMJVV_M8YqRRTQnQrY5baLYHL4tmn_67GcMU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP832479.RAYGLKGBFtMJVV_M8YqRRTQnQrY5baLYHL4tmn_67GcMU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP832479.RAYGLKGBFtMJVV_M8YqRRTQnQrY5baLYHL4tmn_67GcMU130_provenance.
- NP832479.RAYGLKGBFtMJVV_M8YqRRTQnQrY5baLYHL4tmn_67GcMU130_assertion description "[Complex phenotypes have been described in association with MFN2 gene mutations, including CMT2 with pyramidal features (hereditary motor and sensory neuropathy [HSMN V]) and CMT2 with optic atrophy (HMSN VI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP832479.RAYGLKGBFtMJVV_M8YqRRTQnQrY5baLYHL4tmn_67GcMU130_provenance.
- NP832479.RAYGLKGBFtMJVV_M8YqRRTQnQrY5baLYHL4tmn_67GcMU130_assertion evidence source_evidence_literature NP832479.RAYGLKGBFtMJVV_M8YqRRTQnQrY5baLYHL4tmn_67GcMU130_provenance.
- NP832479.RAYGLKGBFtMJVV_M8YqRRTQnQrY5baLYHL4tmn_67GcMU130_assertion SIO_000772 18946002 NP832479.RAYGLKGBFtMJVV_M8YqRRTQnQrY5baLYHL4tmn_67GcMU130_provenance.
- NP832479.RAYGLKGBFtMJVV_M8YqRRTQnQrY5baLYHL4tmn_67GcMU130_assertion wasDerivedFrom befree-20150227 NP832479.RAYGLKGBFtMJVV_M8YqRRTQnQrY5baLYHL4tmn_67GcMU130_provenance.
- NP832479.RAYGLKGBFtMJVV_M8YqRRTQnQrY5baLYHL4tmn_67GcMU130_assertion wasGeneratedBy ECO_0000203 NP832479.RAYGLKGBFtMJVV_M8YqRRTQnQrY5baLYHL4tmn_67GcMU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP832479.RAYGLKGBFtMJVV_M8YqRRTQnQrY5baLYHL4tmn_67GcMU130_provenance.