Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_assertion> ?p ?o ?g. }
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- NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_assertion type Assertion NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_head.
- NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_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." NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_provenance.
- NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_assertion evidence source_evidence_literature NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_provenance.
- NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_assertion SIO_000772 8895241 NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_provenance.
- NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_assertion wasDerivedFrom befree-20140225 NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_provenance.
- NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_assertion wasGeneratedBy ECO_0000203 NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_provenance.