Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1097903.RAqSx2OxmcQW2aVFhb1IlzMw1CxNitUmPfzGcSAS5h0cU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1097903.RAqSx2OxmcQW2aVFhb1IlzMw1CxNitUmPfzGcSAS5h0cU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1097903.RAqSx2OxmcQW2aVFhb1IlzMw1CxNitUmPfzGcSAS5h0cU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1097903.RAqSx2OxmcQW2aVFhb1IlzMw1CxNitUmPfzGcSAS5h0cU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1097903.RAqSx2OxmcQW2aVFhb1IlzMw1CxNitUmPfzGcSAS5h0cU130_provenance.
- NP1097903.RAqSx2OxmcQW2aVFhb1IlzMw1CxNitUmPfzGcSAS5h0cU130_assertion wasGeneratedBy ECO_0000203 NP1097903.RAqSx2OxmcQW2aVFhb1IlzMw1CxNitUmPfzGcSAS5h0cU130_provenance.
- NP1097903.RAqSx2OxmcQW2aVFhb1IlzMw1CxNitUmPfzGcSAS5h0cU130_assertion wasDerivedFrom befree-2016 NP1097903.RAqSx2OxmcQW2aVFhb1IlzMw1CxNitUmPfzGcSAS5h0cU130_provenance.
- NP1097903.RAqSx2OxmcQW2aVFhb1IlzMw1CxNitUmPfzGcSAS5h0cU130_assertion SIO_000772 23897027 NP1097903.RAqSx2OxmcQW2aVFhb1IlzMw1CxNitUmPfzGcSAS5h0cU130_provenance.
- NP1097903.RAqSx2OxmcQW2aVFhb1IlzMw1CxNitUmPfzGcSAS5h0cU130_assertion evidence source_evidence_literature NP1097903.RAqSx2OxmcQW2aVFhb1IlzMw1CxNitUmPfzGcSAS5h0cU130_provenance.
- NP1097903.RAqSx2OxmcQW2aVFhb1IlzMw1CxNitUmPfzGcSAS5h0cU130_assertion description "[SPG2/Proteolipid protein and SPG42/Connexin 47); (5) protein folding and ER-stress response (SPG6/NIPA1, SPG8/K1AA0196 (Strumpellin), SGP17/BSCL2 (Seipin), mutilating sensory neuropathy with spastic paraplegia owing to CcT5 mutation and presumably SPG18/ERLIN2); (6) corticospinal tract and other neurodevelopment (e.g.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1097903.RAqSx2OxmcQW2aVFhb1IlzMw1CxNitUmPfzGcSAS5h0cU130_provenance.