Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP755135.RAoar37hIYZXdL9ISdW3bm1fzmU4f9C-_8aTEEq3f9K18130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP755135.RAoar37hIYZXdL9ISdW3bm1fzmU4f9C-_8aTEEq3f9K18130_assertion type Assertion NP755135.RAoar37hIYZXdL9ISdW3bm1fzmU4f9C-_8aTEEq3f9K18130_head.
- NP755135.RAoar37hIYZXdL9ISdW3bm1fzmU4f9C-_8aTEEq3f9K18130_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." NP755135.RAoar37hIYZXdL9ISdW3bm1fzmU4f9C-_8aTEEq3f9K18130_provenance.
- NP755135.RAoar37hIYZXdL9ISdW3bm1fzmU4f9C-_8aTEEq3f9K18130_assertion evidence source_evidence_literature NP755135.RAoar37hIYZXdL9ISdW3bm1fzmU4f9C-_8aTEEq3f9K18130_provenance.
- NP755135.RAoar37hIYZXdL9ISdW3bm1fzmU4f9C-_8aTEEq3f9K18130_assertion SIO_000772 19651702 NP755135.RAoar37hIYZXdL9ISdW3bm1fzmU4f9C-_8aTEEq3f9K18130_provenance.
- NP755135.RAoar37hIYZXdL9ISdW3bm1fzmU4f9C-_8aTEEq3f9K18130_assertion wasDerivedFrom befree-2016 NP755135.RAoar37hIYZXdL9ISdW3bm1fzmU4f9C-_8aTEEq3f9K18130_provenance.
- NP755135.RAoar37hIYZXdL9ISdW3bm1fzmU4f9C-_8aTEEq3f9K18130_assertion wasGeneratedBy ECO_0000203 NP755135.RAoar37hIYZXdL9ISdW3bm1fzmU4f9C-_8aTEEq3f9K18130_provenance.