Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP864979.RApstRmlz_lOCFGpxqDGR5y99RVtjGXaSvGVadR3SXIHg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP864979.RApstRmlz_lOCFGpxqDGR5y99RVtjGXaSvGVadR3SXIHg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP864979.RApstRmlz_lOCFGpxqDGR5y99RVtjGXaSvGVadR3SXIHg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP864979.RApstRmlz_lOCFGpxqDGR5y99RVtjGXaSvGVadR3SXIHg130_provenance.
- NP864979.RApstRmlz_lOCFGpxqDGR5y99RVtjGXaSvGVadR3SXIHg130_assertion wasGeneratedBy ECO_0000203 NP864979.RApstRmlz_lOCFGpxqDGR5y99RVtjGXaSvGVadR3SXIHg130_provenance.
- NP864979.RApstRmlz_lOCFGpxqDGR5y99RVtjGXaSvGVadR3SXIHg130_assertion wasDerivedFrom befree-20140225 NP864979.RApstRmlz_lOCFGpxqDGR5y99RVtjGXaSvGVadR3SXIHg130_provenance.
- NP864979.RApstRmlz_lOCFGpxqDGR5y99RVtjGXaSvGVadR3SXIHg130_assertion SIO_000772 17855451 NP864979.RApstRmlz_lOCFGpxqDGR5y99RVtjGXaSvGVadR3SXIHg130_provenance.
- NP864979.RApstRmlz_lOCFGpxqDGR5y99RVtjGXaSvGVadR3SXIHg130_assertion evidence source_evidence_literature NP864979.RApstRmlz_lOCFGpxqDGR5y99RVtjGXaSvGVadR3SXIHg130_provenance.
- NP864979.RApstRmlz_lOCFGpxqDGR5y99RVtjGXaSvGVadR3SXIHg130_assertion description "[Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome and Hirschsprung disease (PCWH) is a complex neurocristopathy caused by SOX10 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP864979.RApstRmlz_lOCFGpxqDGR5y99RVtjGXaSvGVadR3SXIHg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP864979.RApstRmlz_lOCFGpxqDGR5y99RVtjGXaSvGVadR3SXIHg130_provenance.