Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP554814.RAitZZg3zqsvhimI8CRyV7F3WZ_woZkvev8N52ryn_ZVQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP554814.RAitZZg3zqsvhimI8CRyV7F3WZ_woZkvev8N52ryn_ZVQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP554814.RAitZZg3zqsvhimI8CRyV7F3WZ_woZkvev8N52ryn_ZVQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP554814.RAitZZg3zqsvhimI8CRyV7F3WZ_woZkvev8N52ryn_ZVQ130_provenance.
- NP554814.RAitZZg3zqsvhimI8CRyV7F3WZ_woZkvev8N52ryn_ZVQ130_assertion description "[Some mutations, most notably in P0, GJB1, ganglioside-induced differentiation-associated protein 1 (GDAP1), neurofilament light chain (NF-L), and dynamin 2 (DNM2), can result in demyelinating or axonal neuropathies introducing additional complexity in the pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP554814.RAitZZg3zqsvhimI8CRyV7F3WZ_woZkvev8N52ryn_ZVQ130_provenance.
- NP554814.RAitZZg3zqsvhimI8CRyV7F3WZ_woZkvev8N52ryn_ZVQ130_assertion evidence source_evidence_literature NP554814.RAitZZg3zqsvhimI8CRyV7F3WZ_woZkvev8N52ryn_ZVQ130_provenance.
- NP554814.RAitZZg3zqsvhimI8CRyV7F3WZ_woZkvev8N52ryn_ZVQ130_assertion SIO_000772 16775378 NP554814.RAitZZg3zqsvhimI8CRyV7F3WZ_woZkvev8N52ryn_ZVQ130_provenance.
- NP554814.RAitZZg3zqsvhimI8CRyV7F3WZ_woZkvev8N52ryn_ZVQ130_assertion wasDerivedFrom befree-2016 NP554814.RAitZZg3zqsvhimI8CRyV7F3WZ_woZkvev8N52ryn_ZVQ130_provenance.
- NP554814.RAitZZg3zqsvhimI8CRyV7F3WZ_woZkvev8N52ryn_ZVQ130_assertion wasGeneratedBy ECO_0000203 NP554814.RAitZZg3zqsvhimI8CRyV7F3WZ_woZkvev8N52ryn_ZVQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP554814.RAitZZg3zqsvhimI8CRyV7F3WZ_woZkvev8N52ryn_ZVQ130_provenance.