Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP708905.RAX1euiO6NSvHxgJrhVM6Yi0K7fyTeVeAMvPYAlkXGO9s130_assertion> ?p ?o ?g. }
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- NP708905.RAX1euiO6NSvHxgJrhVM6Yi0K7fyTeVeAMvPYAlkXGO9s130_assertion type Assertion NP708905.RAX1euiO6NSvHxgJrhVM6Yi0K7fyTeVeAMvPYAlkXGO9s130_head.
- NP708905.RAX1euiO6NSvHxgJrhVM6Yi0K7fyTeVeAMvPYAlkXGO9s130_assertion wasGeneratedBy ECO_0000203 NP708905.RAX1euiO6NSvHxgJrhVM6Yi0K7fyTeVeAMvPYAlkXGO9s130_provenance.
- NP708905.RAX1euiO6NSvHxgJrhVM6Yi0K7fyTeVeAMvPYAlkXGO9s130_assertion wasDerivedFrom befree-20150227 NP708905.RAX1euiO6NSvHxgJrhVM6Yi0K7fyTeVeAMvPYAlkXGO9s130_provenance.
- NP708905.RAX1euiO6NSvHxgJrhVM6Yi0K7fyTeVeAMvPYAlkXGO9s130_assertion SIO_000772 17855451 NP708905.RAX1euiO6NSvHxgJrhVM6Yi0K7fyTeVeAMvPYAlkXGO9s130_provenance.
- NP708905.RAX1euiO6NSvHxgJrhVM6Yi0K7fyTeVeAMvPYAlkXGO9s130_assertion evidence source_evidence_literature NP708905.RAX1euiO6NSvHxgJrhVM6Yi0K7fyTeVeAMvPYAlkXGO9s130_provenance.
- NP708905.RAX1euiO6NSvHxgJrhVM6Yi0K7fyTeVeAMvPYAlkXGO9s130_assertion description "[Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome and Hirschsprung disease (PCWH) is a complex neurocristopathy caused by SOX10 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708905.RAX1euiO6NSvHxgJrhVM6Yi0K7fyTeVeAMvPYAlkXGO9s130_provenance.