Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP755132.RAY_D0nP4K8VvgGiygnjqsYetAk2r8G3g7vZIjOZfAVQ8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP755132.RAY_D0nP4K8VvgGiygnjqsYetAk2r8G3g7vZIjOZfAVQ8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP755132.RAY_D0nP4K8VvgGiygnjqsYetAk2r8G3g7vZIjOZfAVQ8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP755132.RAY_D0nP4K8VvgGiygnjqsYetAk2r8G3g7vZIjOZfAVQ8130_provenance.
- NP755132.RAY_D0nP4K8VvgGiygnjqsYetAk2r8G3g7vZIjOZfAVQ8130_assertion description "[The phenotypes associated with mutations in NTRK1 and WNK1/HSN2 typically consisted of congenital insensitivity to pain and anhidrosis, and early-onset ulcero-mutilating sensory neuropathy, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755132.RAY_D0nP4K8VvgGiygnjqsYetAk2r8G3g7vZIjOZfAVQ8130_provenance.
- NP755132.RAY_D0nP4K8VvgGiygnjqsYetAk2r8G3g7vZIjOZfAVQ8130_assertion evidence source_evidence_literature NP755132.RAY_D0nP4K8VvgGiygnjqsYetAk2r8G3g7vZIjOZfAVQ8130_provenance.
- NP755132.RAY_D0nP4K8VvgGiygnjqsYetAk2r8G3g7vZIjOZfAVQ8130_assertion SIO_000772 19651702 NP755132.RAY_D0nP4K8VvgGiygnjqsYetAk2r8G3g7vZIjOZfAVQ8130_provenance.
- NP755132.RAY_D0nP4K8VvgGiygnjqsYetAk2r8G3g7vZIjOZfAVQ8130_assertion wasDerivedFrom befree-2016 NP755132.RAY_D0nP4K8VvgGiygnjqsYetAk2r8G3g7vZIjOZfAVQ8130_provenance.
- NP755132.RAY_D0nP4K8VvgGiygnjqsYetAk2r8G3g7vZIjOZfAVQ8130_assertion wasGeneratedBy ECO_0000203 NP755132.RAY_D0nP4K8VvgGiygnjqsYetAk2r8G3g7vZIjOZfAVQ8130_provenance.
- befree-2016 importedOn "2016-02-19" NP755132.RAY_D0nP4K8VvgGiygnjqsYetAk2r8G3g7vZIjOZfAVQ8130_provenance.