Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP600176.RA4k6KzAVa2FJwWsLrghq52OZcPTUL7GpvQLVxKzbcWLE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP600176.RA4k6KzAVa2FJwWsLrghq52OZcPTUL7GpvQLVxKzbcWLE130_assertion type Assertion NP600176.RA4k6KzAVa2FJwWsLrghq52OZcPTUL7GpvQLVxKzbcWLE130_head.
- NP600176.RA4k6KzAVa2FJwWsLrghq52OZcPTUL7GpvQLVxKzbcWLE130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600176.RA4k6KzAVa2FJwWsLrghq52OZcPTUL7GpvQLVxKzbcWLE130_provenance.
- NP600176.RA4k6KzAVa2FJwWsLrghq52OZcPTUL7GpvQLVxKzbcWLE130_assertion evidence source_evidence_literature NP600176.RA4k6KzAVa2FJwWsLrghq52OZcPTUL7GpvQLVxKzbcWLE130_provenance.
- NP600176.RA4k6KzAVa2FJwWsLrghq52OZcPTUL7GpvQLVxKzbcWLE130_assertion SIO_000772 8895241 NP600176.RA4k6KzAVa2FJwWsLrghq52OZcPTUL7GpvQLVxKzbcWLE130_provenance.
- NP600176.RA4k6KzAVa2FJwWsLrghq52OZcPTUL7GpvQLVxKzbcWLE130_assertion wasDerivedFrom befree-20150227 NP600176.RA4k6KzAVa2FJwWsLrghq52OZcPTUL7GpvQLVxKzbcWLE130_provenance.
- NP600176.RA4k6KzAVa2FJwWsLrghq52OZcPTUL7GpvQLVxKzbcWLE130_assertion wasGeneratedBy ECO_0000203 NP600176.RA4k6KzAVa2FJwWsLrghq52OZcPTUL7GpvQLVxKzbcWLE130_provenance.