Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP629984.RAyUSSvnIrvgWvCM7QMmmZF6Xk-jinUvHNYycOLWgnBkE130_assertion> ?p ?o ?g. }
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- NP629984.RAyUSSvnIrvgWvCM7QMmmZF6Xk-jinUvHNYycOLWgnBkE130_assertion type Assertion NP629984.RAyUSSvnIrvgWvCM7QMmmZF6Xk-jinUvHNYycOLWgnBkE130_head.
- NP629984.RAyUSSvnIrvgWvCM7QMmmZF6Xk-jinUvHNYycOLWgnBkE130_assertion wasGeneratedBy ECO_0000203 NP629984.RAyUSSvnIrvgWvCM7QMmmZF6Xk-jinUvHNYycOLWgnBkE130_provenance.
- NP629984.RAyUSSvnIrvgWvCM7QMmmZF6Xk-jinUvHNYycOLWgnBkE130_assertion wasDerivedFrom befree-2016 NP629984.RAyUSSvnIrvgWvCM7QMmmZF6Xk-jinUvHNYycOLWgnBkE130_provenance.
- NP629984.RAyUSSvnIrvgWvCM7QMmmZF6Xk-jinUvHNYycOLWgnBkE130_assertion SIO_000772 17855451 NP629984.RAyUSSvnIrvgWvCM7QMmmZF6Xk-jinUvHNYycOLWgnBkE130_provenance.
- NP629984.RAyUSSvnIrvgWvCM7QMmmZF6Xk-jinUvHNYycOLWgnBkE130_assertion evidence source_evidence_literature NP629984.RAyUSSvnIrvgWvCM7QMmmZF6Xk-jinUvHNYycOLWgnBkE130_provenance.
- NP629984.RAyUSSvnIrvgWvCM7QMmmZF6Xk-jinUvHNYycOLWgnBkE130_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." NP629984.RAyUSSvnIrvgWvCM7QMmmZF6Xk-jinUvHNYycOLWgnBkE130_provenance.