Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP8906.RACo6RXNq5PEWVN0K_VC5DMbY0YIiAW3YKg31_QW1-gxY130_assertion> ?p ?o ?g. }
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- NP8906.RACo6RXNq5PEWVN0K_VC5DMbY0YIiAW3YKg31_QW1-gxY130_assertion type Assertion NP8906.RACo6RXNq5PEWVN0K_VC5DMbY0YIiAW3YKg31_QW1-gxY130_head.
- NP8906.RACo6RXNq5PEWVN0K_VC5DMbY0YIiAW3YKg31_QW1-gxY130_assertion wasGeneratedBy ECO_0000218 NP8906.RACo6RXNq5PEWVN0K_VC5DMbY0YIiAW3YKg31_QW1-gxY130_provenance.
- NP8906.RACo6RXNq5PEWVN0K_VC5DMbY0YIiAW3YKg31_QW1-gxY130_assertion wasDerivedFrom uniprot-2016 NP8906.RACo6RXNq5PEWVN0K_VC5DMbY0YIiAW3YKg31_QW1-gxY130_provenance.
- NP8906.RACo6RXNq5PEWVN0K_VC5DMbY0YIiAW3YKg31_QW1-gxY130_assertion SIO_000772 8447316 NP8906.RACo6RXNq5PEWVN0K_VC5DMbY0YIiAW3YKg31_QW1-gxY130_provenance.
- NP8906.RACo6RXNq5PEWVN0K_VC5DMbY0YIiAW3YKg31_QW1-gxY130_assertion evidence source_evidence_curated NP8906.RACo6RXNq5PEWVN0K_VC5DMbY0YIiAW3YKg31_QW1-gxY130_provenance.
- NP8906.RACo6RXNq5PEWVN0K_VC5DMbY0YIiAW3YKg31_QW1-gxY130_assertion description "[Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8906.RACo6RXNq5PEWVN0K_VC5DMbY0YIiAW3YKg31_QW1-gxY130_provenance.