Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP386794.RAPhRlxj1Cj51lL_kEUyQHtVY-0ktUL4AzHNBKRSZLY7U130_assertion> ?p ?o ?g. }
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- NP386794.RAPhRlxj1Cj51lL_kEUyQHtVY-0ktUL4AzHNBKRSZLY7U130_assertion type Assertion NP386794.RAPhRlxj1Cj51lL_kEUyQHtVY-0ktUL4AzHNBKRSZLY7U130_head.
- NP386794.RAPhRlxj1Cj51lL_kEUyQHtVY-0ktUL4AzHNBKRSZLY7U130_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." NP386794.RAPhRlxj1Cj51lL_kEUyQHtVY-0ktUL4AzHNBKRSZLY7U130_provenance.
- NP386794.RAPhRlxj1Cj51lL_kEUyQHtVY-0ktUL4AzHNBKRSZLY7U130_assertion evidence source_evidence_literature NP386794.RAPhRlxj1Cj51lL_kEUyQHtVY-0ktUL4AzHNBKRSZLY7U130_provenance.
- NP386794.RAPhRlxj1Cj51lL_kEUyQHtVY-0ktUL4AzHNBKRSZLY7U130_assertion SIO_000772 19651702 NP386794.RAPhRlxj1Cj51lL_kEUyQHtVY-0ktUL4AzHNBKRSZLY7U130_provenance.
- NP386794.RAPhRlxj1Cj51lL_kEUyQHtVY-0ktUL4AzHNBKRSZLY7U130_assertion wasDerivedFrom befree-20140225 NP386794.RAPhRlxj1Cj51lL_kEUyQHtVY-0ktUL4AzHNBKRSZLY7U130_provenance.
- NP386794.RAPhRlxj1Cj51lL_kEUyQHtVY-0ktUL4AzHNBKRSZLY7U130_assertion wasGeneratedBy ECO_0000203 NP386794.RAPhRlxj1Cj51lL_kEUyQHtVY-0ktUL4AzHNBKRSZLY7U130_provenance.