Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP572074.RAm4JAUNkwk1KALTbY14G9OT8wegMlCP2EcQpVg6c5K_Y130_assertion> ?p ?o ?g. }
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- NP572074.RAm4JAUNkwk1KALTbY14G9OT8wegMlCP2EcQpVg6c5K_Y130_assertion type Assertion NP572074.RAm4JAUNkwk1KALTbY14G9OT8wegMlCP2EcQpVg6c5K_Y130_head.
- NP572074.RAm4JAUNkwk1KALTbY14G9OT8wegMlCP2EcQpVg6c5K_Y130_assertion wasGeneratedBy ECO_0000203 NP572074.RAm4JAUNkwk1KALTbY14G9OT8wegMlCP2EcQpVg6c5K_Y130_provenance.
- NP572074.RAm4JAUNkwk1KALTbY14G9OT8wegMlCP2EcQpVg6c5K_Y130_assertion wasDerivedFrom befree-20140225 NP572074.RAm4JAUNkwk1KALTbY14G9OT8wegMlCP2EcQpVg6c5K_Y130_provenance.
- NP572074.RAm4JAUNkwk1KALTbY14G9OT8wegMlCP2EcQpVg6c5K_Y130_assertion SIO_000772 17855451 NP572074.RAm4JAUNkwk1KALTbY14G9OT8wegMlCP2EcQpVg6c5K_Y130_provenance.
- NP572074.RAm4JAUNkwk1KALTbY14G9OT8wegMlCP2EcQpVg6c5K_Y130_assertion evidence source_evidence_literature NP572074.RAm4JAUNkwk1KALTbY14G9OT8wegMlCP2EcQpVg6c5K_Y130_provenance.
- NP572074.RAm4JAUNkwk1KALTbY14G9OT8wegMlCP2EcQpVg6c5K_Y130_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." NP572074.RAm4JAUNkwk1KALTbY14G9OT8wegMlCP2EcQpVg6c5K_Y130_provenance.