Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP315468.RAn-IQVUfgy43FaHYf9TwTohqoZnVgbnw0gmFXtP_Tc_E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP315468.RAn-IQVUfgy43FaHYf9TwTohqoZnVgbnw0gmFXtP_Tc_E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP315468.RAn-IQVUfgy43FaHYf9TwTohqoZnVgbnw0gmFXtP_Tc_E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP315468.RAn-IQVUfgy43FaHYf9TwTohqoZnVgbnw0gmFXtP_Tc_E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP315468.RAn-IQVUfgy43FaHYf9TwTohqoZnVgbnw0gmFXtP_Tc_E130_provenance.
- 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.