Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP199345.RAGyx1oiR3cUQDTvpVHlBluJF1JIPK_C7Ihe0EpUOpJHs130_assertion> ?p ?o ?g. }
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- NP199345.RAGyx1oiR3cUQDTvpVHlBluJF1JIPK_C7Ihe0EpUOpJHs130_assertion type Assertion NP199345.RAGyx1oiR3cUQDTvpVHlBluJF1JIPK_C7Ihe0EpUOpJHs130_head.
- NP199345.RAGyx1oiR3cUQDTvpVHlBluJF1JIPK_C7Ihe0EpUOpJHs130_assertion description "[the first description of a mutation in cytoskeletal, or nonmuscle, actin; with an autosomal dominant, progressive, sensorineural hearing loss phenotype ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199345.RAGyx1oiR3cUQDTvpVHlBluJF1JIPK_C7Ihe0EpUOpJHs130_provenance.
- NP199345.RAGyx1oiR3cUQDTvpVHlBluJF1JIPK_C7Ihe0EpUOpJHs130_assertion evidence source_evidence_literature NP199345.RAGyx1oiR3cUQDTvpVHlBluJF1JIPK_C7Ihe0EpUOpJHs130_provenance.
- NP199345.RAGyx1oiR3cUQDTvpVHlBluJF1JIPK_C7Ihe0EpUOpJHs130_assertion SIO_000772 13680526 NP199345.RAGyx1oiR3cUQDTvpVHlBluJF1JIPK_C7Ihe0EpUOpJHs130_provenance.
- NP199345.RAGyx1oiR3cUQDTvpVHlBluJF1JIPK_C7Ihe0EpUOpJHs130_assertion wasDerivedFrom lhgdn-20090331 NP199345.RAGyx1oiR3cUQDTvpVHlBluJF1JIPK_C7Ihe0EpUOpJHs130_provenance.
- NP199345.RAGyx1oiR3cUQDTvpVHlBluJF1JIPK_C7Ihe0EpUOpJHs130_assertion wasGeneratedBy ECO_0000203 NP199345.RAGyx1oiR3cUQDTvpVHlBluJF1JIPK_C7Ihe0EpUOpJHs130_provenance.