Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP408156.RAVRfei7Z_KGZu_1UcHoSo5b3WPgJbuaAc3Fld0zrf_Xs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP408156.RAVRfei7Z_KGZu_1UcHoSo5b3WPgJbuaAc3Fld0zrf_Xs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP408156.RAVRfei7Z_KGZu_1UcHoSo5b3WPgJbuaAc3Fld0zrf_Xs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP408156.RAVRfei7Z_KGZu_1UcHoSo5b3WPgJbuaAc3Fld0zrf_Xs130_provenance.
- NP408156.RAVRfei7Z_KGZu_1UcHoSo5b3WPgJbuaAc3Fld0zrf_Xs130_assertion wasGeneratedBy ECO_0000203 NP408156.RAVRfei7Z_KGZu_1UcHoSo5b3WPgJbuaAc3Fld0zrf_Xs130_provenance.
- NP408156.RAVRfei7Z_KGZu_1UcHoSo5b3WPgJbuaAc3Fld0zrf_Xs130_assertion wasDerivedFrom befree-20140225 NP408156.RAVRfei7Z_KGZu_1UcHoSo5b3WPgJbuaAc3Fld0zrf_Xs130_provenance.
- NP408156.RAVRfei7Z_KGZu_1UcHoSo5b3WPgJbuaAc3Fld0zrf_Xs130_assertion SIO_000772 18310267 NP408156.RAVRfei7Z_KGZu_1UcHoSo5b3WPgJbuaAc3Fld0zrf_Xs130_provenance.
- NP408156.RAVRfei7Z_KGZu_1UcHoSo5b3WPgJbuaAc3Fld0zrf_Xs130_assertion evidence source_evidence_literature NP408156.RAVRfei7Z_KGZu_1UcHoSo5b3WPgJbuaAc3Fld0zrf_Xs130_provenance.
- NP408156.RAVRfei7Z_KGZu_1UcHoSo5b3WPgJbuaAc3Fld0zrf_Xs130_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." NP408156.RAVRfei7Z_KGZu_1UcHoSo5b3WPgJbuaAc3Fld0zrf_Xs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP408156.RAVRfei7Z_KGZu_1UcHoSo5b3WPgJbuaAc3Fld0zrf_Xs130_provenance.