Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP869988.RA_zQCnAcr4TjPkk_1s-C6lU-CCCINnxP9T3EbL9P9-VA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP869988.RA_zQCnAcr4TjPkk_1s-C6lU-CCCINnxP9T3EbL9P9-VA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869988.RA_zQCnAcr4TjPkk_1s-C6lU-CCCINnxP9T3EbL9P9-VA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869988.RA_zQCnAcr4TjPkk_1s-C6lU-CCCINnxP9T3EbL9P9-VA130_provenance.
- NP869988.RA_zQCnAcr4TjPkk_1s-C6lU-CCCINnxP9T3EbL9P9-VA130_assertion description "[Mutations in the SH3TC2 gene are a frequent cause of demyelinating hereditary neuropathy among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869988.RA_zQCnAcr4TjPkk_1s-C6lU-CCCINnxP9T3EbL9P9-VA130_provenance.
- NP869988.RA_zQCnAcr4TjPkk_1s-C6lU-CCCINnxP9T3EbL9P9-VA130_assertion evidence source_evidence_literature NP869988.RA_zQCnAcr4TjPkk_1s-C6lU-CCCINnxP9T3EbL9P9-VA130_provenance.
- NP869988.RA_zQCnAcr4TjPkk_1s-C6lU-CCCINnxP9T3EbL9P9-VA130_assertion SIO_000772 21291453 NP869988.RA_zQCnAcr4TjPkk_1s-C6lU-CCCINnxP9T3EbL9P9-VA130_provenance.
- NP869988.RA_zQCnAcr4TjPkk_1s-C6lU-CCCINnxP9T3EbL9P9-VA130_assertion wasDerivedFrom befree-2016 NP869988.RA_zQCnAcr4TjPkk_1s-C6lU-CCCINnxP9T3EbL9P9-VA130_provenance.
- NP869988.RA_zQCnAcr4TjPkk_1s-C6lU-CCCINnxP9T3EbL9P9-VA130_assertion wasGeneratedBy ECO_0000203 NP869988.RA_zQCnAcr4TjPkk_1s-C6lU-CCCINnxP9T3EbL9P9-VA130_provenance.
- befree-2016 importedOn "2016-02-19" NP869988.RA_zQCnAcr4TjPkk_1s-C6lU-CCCINnxP9T3EbL9P9-VA130_provenance.