Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP916729.RAAUsGKV8744Ute8dVU2DRsUVG7DR-1GhLmmypQSUFxDQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP916729.RAAUsGKV8744Ute8dVU2DRsUVG7DR-1GhLmmypQSUFxDQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP916729.RAAUsGKV8744Ute8dVU2DRsUVG7DR-1GhLmmypQSUFxDQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP916729.RAAUsGKV8744Ute8dVU2DRsUVG7DR-1GhLmmypQSUFxDQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP916729.RAAUsGKV8744Ute8dVU2DRsUVG7DR-1GhLmmypQSUFxDQ130_provenance.
- NP916729.RAAUsGKV8744Ute8dVU2DRsUVG7DR-1GhLmmypQSUFxDQ130_assertion wasGeneratedBy ECO_0000203 NP916729.RAAUsGKV8744Ute8dVU2DRsUVG7DR-1GhLmmypQSUFxDQ130_provenance.
- NP916729.RAAUsGKV8744Ute8dVU2DRsUVG7DR-1GhLmmypQSUFxDQ130_assertion wasDerivedFrom befree-2016 NP916729.RAAUsGKV8744Ute8dVU2DRsUVG7DR-1GhLmmypQSUFxDQ130_provenance.
- NP916729.RAAUsGKV8744Ute8dVU2DRsUVG7DR-1GhLmmypQSUFxDQ130_assertion SIO_000772 21838520 NP916729.RAAUsGKV8744Ute8dVU2DRsUVG7DR-1GhLmmypQSUFxDQ130_provenance.
- NP916729.RAAUsGKV8744Ute8dVU2DRsUVG7DR-1GhLmmypQSUFxDQ130_assertion evidence source_evidence_literature NP916729.RAAUsGKV8744Ute8dVU2DRsUVG7DR-1GhLmmypQSUFxDQ130_provenance.
- NP916729.RAAUsGKV8744Ute8dVU2DRsUVG7DR-1GhLmmypQSUFxDQ130_assertion description "[In this study, the aim of prenatal screening was to estimate the carrier frequency of the three mutations 35delG, del (GJB6-D13S1830), and del (GJB6-D13S1854), which are known to be the leading mutations of hereditary hearing loss in European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916729.RAAUsGKV8744Ute8dVU2DRsUVG7DR-1GhLmmypQSUFxDQ130_provenance.