Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP568983.RAdEtjNrWWK03qpFaWMTtTgQuP-FF0S9uMCh8Bo12jBCc130_assertion> ?p ?o ?g. }
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- NP568983.RAdEtjNrWWK03qpFaWMTtTgQuP-FF0S9uMCh8Bo12jBCc130_assertion type Assertion NP568983.RAdEtjNrWWK03qpFaWMTtTgQuP-FF0S9uMCh8Bo12jBCc130_head.
- NP568983.RAdEtjNrWWK03qpFaWMTtTgQuP-FF0S9uMCh8Bo12jBCc130_assertion wasGeneratedBy ECO_0000203 NP568983.RAdEtjNrWWK03qpFaWMTtTgQuP-FF0S9uMCh8Bo12jBCc130_provenance.
- NP568983.RAdEtjNrWWK03qpFaWMTtTgQuP-FF0S9uMCh8Bo12jBCc130_assertion wasDerivedFrom befree-20140225 NP568983.RAdEtjNrWWK03qpFaWMTtTgQuP-FF0S9uMCh8Bo12jBCc130_provenance.
- NP568983.RAdEtjNrWWK03qpFaWMTtTgQuP-FF0S9uMCh8Bo12jBCc130_assertion SIO_000772 21965087 NP568983.RAdEtjNrWWK03qpFaWMTtTgQuP-FF0S9uMCh8Bo12jBCc130_provenance.
- NP568983.RAdEtjNrWWK03qpFaWMTtTgQuP-FF0S9uMCh8Bo12jBCc130_assertion evidence source_evidence_literature NP568983.RAdEtjNrWWK03qpFaWMTtTgQuP-FF0S9uMCh8Bo12jBCc130_provenance.
- NP568983.RAdEtjNrWWK03qpFaWMTtTgQuP-FF0S9uMCh8Bo12jBCc130_assertion description "[Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568983.RAdEtjNrWWK03qpFaWMTtTgQuP-FF0S9uMCh8Bo12jBCc130_provenance.