Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP941120.RAi7ACfYq0V-250oAIm2rlffHj7uo4WZTWagrO0U-8xFQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP941120.RAi7ACfYq0V-250oAIm2rlffHj7uo4WZTWagrO0U-8xFQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP941120.RAi7ACfYq0V-250oAIm2rlffHj7uo4WZTWagrO0U-8xFQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP941120.RAi7ACfYq0V-250oAIm2rlffHj7uo4WZTWagrO0U-8xFQ130_provenance.
- NP941120.RAi7ACfYq0V-250oAIm2rlffHj7uo4WZTWagrO0U-8xFQ130_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." NP941120.RAi7ACfYq0V-250oAIm2rlffHj7uo4WZTWagrO0U-8xFQ130_provenance.
- NP941120.RAi7ACfYq0V-250oAIm2rlffHj7uo4WZTWagrO0U-8xFQ130_assertion evidence source_evidence_literature NP941120.RAi7ACfYq0V-250oAIm2rlffHj7uo4WZTWagrO0U-8xFQ130_provenance.
- NP941120.RAi7ACfYq0V-250oAIm2rlffHj7uo4WZTWagrO0U-8xFQ130_assertion SIO_000772 19651702 NP941120.RAi7ACfYq0V-250oAIm2rlffHj7uo4WZTWagrO0U-8xFQ130_provenance.
- NP941120.RAi7ACfYq0V-250oAIm2rlffHj7uo4WZTWagrO0U-8xFQ130_assertion wasDerivedFrom befree-20150227 NP941120.RAi7ACfYq0V-250oAIm2rlffHj7uo4WZTWagrO0U-8xFQ130_provenance.
- NP941120.RAi7ACfYq0V-250oAIm2rlffHj7uo4WZTWagrO0U-8xFQ130_assertion wasGeneratedBy ECO_0000203 NP941120.RAi7ACfYq0V-250oAIm2rlffHj7uo4WZTWagrO0U-8xFQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP941120.RAi7ACfYq0V-250oAIm2rlffHj7uo4WZTWagrO0U-8xFQ130_provenance.