Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_assertion type Assertion NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_head.
- NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_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." NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_provenance.
- NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_assertion evidence source_evidence_literature NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_provenance.
- NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_assertion SIO_000772 19651702 NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_provenance.
- NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_assertion wasDerivedFrom befree-20150227 NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_provenance.
- NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_assertion wasGeneratedBy ECO_0000203 NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_provenance.