Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP783612.RAKCg1ju6WBKV8OFS6HpRLDw3McGTc8a1CWGRgZziqmDw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783612.RAKCg1ju6WBKV8OFS6HpRLDw3McGTc8a1CWGRgZziqmDw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783612.RAKCg1ju6WBKV8OFS6HpRLDw3McGTc8a1CWGRgZziqmDw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783612.RAKCg1ju6WBKV8OFS6HpRLDw3McGTc8a1CWGRgZziqmDw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP783612.RAKCg1ju6WBKV8OFS6HpRLDw3McGTc8a1CWGRgZziqmDw130_provenance.
- NP783612.RAKCg1ju6WBKV8OFS6HpRLDw3McGTc8a1CWGRgZziqmDw130_assertion wasGeneratedBy ECO_0000203 NP783612.RAKCg1ju6WBKV8OFS6HpRLDw3McGTc8a1CWGRgZziqmDw130_provenance.
- NP783612.RAKCg1ju6WBKV8OFS6HpRLDw3McGTc8a1CWGRgZziqmDw130_assertion wasDerivedFrom befree-20150227 NP783612.RAKCg1ju6WBKV8OFS6HpRLDw3McGTc8a1CWGRgZziqmDw130_provenance.
- NP783612.RAKCg1ju6WBKV8OFS6HpRLDw3McGTc8a1CWGRgZziqmDw130_assertion SIO_000772 18310267 NP783612.RAKCg1ju6WBKV8OFS6HpRLDw3McGTc8a1CWGRgZziqmDw130_provenance.
- NP783612.RAKCg1ju6WBKV8OFS6HpRLDw3McGTc8a1CWGRgZziqmDw130_assertion evidence source_evidence_literature NP783612.RAKCg1ju6WBKV8OFS6HpRLDw3McGTc8a1CWGRgZziqmDw130_provenance.
- NP783612.RAKCg1ju6WBKV8OFS6HpRLDw3McGTc8a1CWGRgZziqmDw130_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." NP783612.RAKCg1ju6WBKV8OFS6HpRLDw3McGTc8a1CWGRgZziqmDw130_provenance.