Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP268034.RABMgl8MPEG61BUaclqXHKxvmOUhhM65GOxfmWT3NT9PI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP268034.RABMgl8MPEG61BUaclqXHKxvmOUhhM65GOxfmWT3NT9PI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP268034.RABMgl8MPEG61BUaclqXHKxvmOUhhM65GOxfmWT3NT9PI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP268034.RABMgl8MPEG61BUaclqXHKxvmOUhhM65GOxfmWT3NT9PI130_provenance.
- NP268034.RABMgl8MPEG61BUaclqXHKxvmOUhhM65GOxfmWT3NT9PI130_assertion description "[Point mutations affecting the NTRK1/TRKA gene, encoding one of the receptors for the nerve growth factor (NGF), have been detected in congenital insensitivity to pain with anhidrosis (CIPA), a human hereditary sensory neuropathy characterized by absence of reaction to noxious stimuli and anhidrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268034.RABMgl8MPEG61BUaclqXHKxvmOUhhM65GOxfmWT3NT9PI130_provenance.
- NP268034.RABMgl8MPEG61BUaclqXHKxvmOUhhM65GOxfmWT3NT9PI130_assertion evidence source_evidence_literature NP268034.RABMgl8MPEG61BUaclqXHKxvmOUhhM65GOxfmWT3NT9PI130_provenance.
- NP268034.RABMgl8MPEG61BUaclqXHKxvmOUhhM65GOxfmWT3NT9PI130_assertion SIO_000772 10567924 NP268034.RABMgl8MPEG61BUaclqXHKxvmOUhhM65GOxfmWT3NT9PI130_provenance.
- NP268034.RABMgl8MPEG61BUaclqXHKxvmOUhhM65GOxfmWT3NT9PI130_assertion wasDerivedFrom befree-2016 NP268034.RABMgl8MPEG61BUaclqXHKxvmOUhhM65GOxfmWT3NT9PI130_provenance.
- NP268034.RABMgl8MPEG61BUaclqXHKxvmOUhhM65GOxfmWT3NT9PI130_assertion wasGeneratedBy ECO_0000203 NP268034.RABMgl8MPEG61BUaclqXHKxvmOUhhM65GOxfmWT3NT9PI130_provenance.
- befree-2016 importedOn "2016-02-19" NP268034.RABMgl8MPEG61BUaclqXHKxvmOUhhM65GOxfmWT3NT9PI130_provenance.