Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP469966.RAuCu8livO5zdshkypdgsdX2oiLaTkiwoYRLto_tx0XvY130_assertion> ?p ?o ?g. }
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- NP469966.RAuCu8livO5zdshkypdgsdX2oiLaTkiwoYRLto_tx0XvY130_assertion type Assertion NP469966.RAuCu8livO5zdshkypdgsdX2oiLaTkiwoYRLto_tx0XvY130_head.
- NP469966.RAuCu8livO5zdshkypdgsdX2oiLaTkiwoYRLto_tx0XvY130_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." NP469966.RAuCu8livO5zdshkypdgsdX2oiLaTkiwoYRLto_tx0XvY130_provenance.
- NP469966.RAuCu8livO5zdshkypdgsdX2oiLaTkiwoYRLto_tx0XvY130_assertion evidence source_evidence_literature NP469966.RAuCu8livO5zdshkypdgsdX2oiLaTkiwoYRLto_tx0XvY130_provenance.
- NP469966.RAuCu8livO5zdshkypdgsdX2oiLaTkiwoYRLto_tx0XvY130_assertion SIO_000772 8895241 NP469966.RAuCu8livO5zdshkypdgsdX2oiLaTkiwoYRLto_tx0XvY130_provenance.
- NP469966.RAuCu8livO5zdshkypdgsdX2oiLaTkiwoYRLto_tx0XvY130_assertion wasDerivedFrom befree-20140225 NP469966.RAuCu8livO5zdshkypdgsdX2oiLaTkiwoYRLto_tx0XvY130_provenance.
- NP469966.RAuCu8livO5zdshkypdgsdX2oiLaTkiwoYRLto_tx0XvY130_assertion wasGeneratedBy ECO_0000203 NP469966.RAuCu8livO5zdshkypdgsdX2oiLaTkiwoYRLto_tx0XvY130_provenance.