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- NP315468.RAn-IQVUfgy43FaHYf9TwTohqoZnVgbnw0gmFXtP_Tc_E130_assertion type Assertion NP315468.RAn-IQVUfgy43FaHYf9TwTohqoZnVgbnw0gmFXtP_Tc_E130_head.
- NP315468.RAn-IQVUfgy43FaHYf9TwTohqoZnVgbnw0gmFXtP_Tc_E130_assertion wasGeneratedBy ECO_0000203 NP315468.RAn-IQVUfgy43FaHYf9TwTohqoZnVgbnw0gmFXtP_Tc_E130_provenance.
- NP315468.RAn-IQVUfgy43FaHYf9TwTohqoZnVgbnw0gmFXtP_Tc_E130_assertion wasDerivedFrom befree-20150227 NP315468.RAn-IQVUfgy43FaHYf9TwTohqoZnVgbnw0gmFXtP_Tc_E130_provenance.
- NP315468.RAn-IQVUfgy43FaHYf9TwTohqoZnVgbnw0gmFXtP_Tc_E130_assertion SIO_000772 18310267 NP315468.RAn-IQVUfgy43FaHYf9TwTohqoZnVgbnw0gmFXtP_Tc_E130_provenance.
- NP315468.RAn-IQVUfgy43FaHYf9TwTohqoZnVgbnw0gmFXtP_Tc_E130_assertion evidence source_evidence_literature NP315468.RAn-IQVUfgy43FaHYf9TwTohqoZnVgbnw0gmFXtP_Tc_E130_provenance.
- NP315468.RAn-IQVUfgy43FaHYf9TwTohqoZnVgbnw0gmFXtP_Tc_E130_assertion description "[BS with sensorineural deafness (SND, OMIM602522) is a newly identified phenotype caused by mutations in the BSND gene that encodes barttin, a beta-subunit for chloride channel ClC-Ka and ClC-Kb and classified as type IV BS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315468.RAn-IQVUfgy43FaHYf9TwTohqoZnVgbnw0gmFXtP_Tc_E130_provenance.