Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP609590.RAGdKDA7fNFJ4FjAb19K6rh2MbuJmK7Ta_0QVTbmEVtcs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP609590.RAGdKDA7fNFJ4FjAb19K6rh2MbuJmK7Ta_0QVTbmEVtcs130_assertion type Assertion NP609590.RAGdKDA7fNFJ4FjAb19K6rh2MbuJmK7Ta_0QVTbmEVtcs130_head.
- NP609590.RAGdKDA7fNFJ4FjAb19K6rh2MbuJmK7Ta_0QVTbmEVtcs130_assertion wasGeneratedBy ECO_0000203 NP609590.RAGdKDA7fNFJ4FjAb19K6rh2MbuJmK7Ta_0QVTbmEVtcs130_provenance.
- NP609590.RAGdKDA7fNFJ4FjAb19K6rh2MbuJmK7Ta_0QVTbmEVtcs130_assertion wasDerivedFrom befree-20150227 NP609590.RAGdKDA7fNFJ4FjAb19K6rh2MbuJmK7Ta_0QVTbmEVtcs130_provenance.
- NP609590.RAGdKDA7fNFJ4FjAb19K6rh2MbuJmK7Ta_0QVTbmEVtcs130_assertion SIO_000772 21965087 NP609590.RAGdKDA7fNFJ4FjAb19K6rh2MbuJmK7Ta_0QVTbmEVtcs130_provenance.
- NP609590.RAGdKDA7fNFJ4FjAb19K6rh2MbuJmK7Ta_0QVTbmEVtcs130_assertion evidence source_evidence_literature NP609590.RAGdKDA7fNFJ4FjAb19K6rh2MbuJmK7Ta_0QVTbmEVtcs130_provenance.
- NP609590.RAGdKDA7fNFJ4FjAb19K6rh2MbuJmK7Ta_0QVTbmEVtcs130_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." NP609590.RAGdKDA7fNFJ4FjAb19K6rh2MbuJmK7Ta_0QVTbmEVtcs130_provenance.