Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP156665.RAy17xueCuMKQPcPXSQasFdVZ2LH8JHn5ZYm1VH_CgKnY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP156665.RAy17xueCuMKQPcPXSQasFdVZ2LH8JHn5ZYm1VH_CgKnY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP156665.RAy17xueCuMKQPcPXSQasFdVZ2LH8JHn5ZYm1VH_CgKnY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP156665.RAy17xueCuMKQPcPXSQasFdVZ2LH8JHn5ZYm1VH_CgKnY130_provenance.
- NP156665.RAy17xueCuMKQPcPXSQasFdVZ2LH8JHn5ZYm1VH_CgKnY130_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." NP156665.RAy17xueCuMKQPcPXSQasFdVZ2LH8JHn5ZYm1VH_CgKnY130_provenance.
- NP156665.RAy17xueCuMKQPcPXSQasFdVZ2LH8JHn5ZYm1VH_CgKnY130_assertion evidence source_evidence_literature NP156665.RAy17xueCuMKQPcPXSQasFdVZ2LH8JHn5ZYm1VH_CgKnY130_provenance.
- NP156665.RAy17xueCuMKQPcPXSQasFdVZ2LH8JHn5ZYm1VH_CgKnY130_assertion SIO_000772 19651702 NP156665.RAy17xueCuMKQPcPXSQasFdVZ2LH8JHn5ZYm1VH_CgKnY130_provenance.
- NP156665.RAy17xueCuMKQPcPXSQasFdVZ2LH8JHn5ZYm1VH_CgKnY130_assertion wasDerivedFrom befree-20140225 NP156665.RAy17xueCuMKQPcPXSQasFdVZ2LH8JHn5ZYm1VH_CgKnY130_provenance.
- NP156665.RAy17xueCuMKQPcPXSQasFdVZ2LH8JHn5ZYm1VH_CgKnY130_assertion wasGeneratedBy ECO_0000203 NP156665.RAy17xueCuMKQPcPXSQasFdVZ2LH8JHn5ZYm1VH_CgKnY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP156665.RAy17xueCuMKQPcPXSQasFdVZ2LH8JHn5ZYm1VH_CgKnY130_provenance.