Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP311076.RACCs_BkbBKx4tkBGkEp4fsivDxEQAVktNwY031SCaUKo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP311076.RACCs_BkbBKx4tkBGkEp4fsivDxEQAVktNwY031SCaUKo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP311076.RACCs_BkbBKx4tkBGkEp4fsivDxEQAVktNwY031SCaUKo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP311076.RACCs_BkbBKx4tkBGkEp4fsivDxEQAVktNwY031SCaUKo130_provenance.
- NP311076.RACCs_BkbBKx4tkBGkEp4fsivDxEQAVktNwY031SCaUKo130_assertion description "[Recently, mutations in the GJB2 gene have been found in a great number of familial and sporadic cases of congenital deafness in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311076.RACCs_BkbBKx4tkBGkEp4fsivDxEQAVktNwY031SCaUKo130_provenance.
- NP311076.RACCs_BkbBKx4tkBGkEp4fsivDxEQAVktNwY031SCaUKo130_assertion evidence source_evidence_literature NP311076.RACCs_BkbBKx4tkBGkEp4fsivDxEQAVktNwY031SCaUKo130_provenance.
- NP311076.RACCs_BkbBKx4tkBGkEp4fsivDxEQAVktNwY031SCaUKo130_assertion SIO_000772 11603757 NP311076.RACCs_BkbBKx4tkBGkEp4fsivDxEQAVktNwY031SCaUKo130_provenance.
- NP311076.RACCs_BkbBKx4tkBGkEp4fsivDxEQAVktNwY031SCaUKo130_assertion wasDerivedFrom befree-20140225 NP311076.RACCs_BkbBKx4tkBGkEp4fsivDxEQAVktNwY031SCaUKo130_provenance.
- NP311076.RACCs_BkbBKx4tkBGkEp4fsivDxEQAVktNwY031SCaUKo130_assertion wasGeneratedBy ECO_0000203 NP311076.RACCs_BkbBKx4tkBGkEp4fsivDxEQAVktNwY031SCaUKo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP311076.RACCs_BkbBKx4tkBGkEp4fsivDxEQAVktNwY031SCaUKo130_provenance.