Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP916729.RAAUsGKV8744Ute8dVU2DRsUVG7DR-1GhLmmypQSUFxDQ130_assertion> ?p ?o ?g. }
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- NP916729.RAAUsGKV8744Ute8dVU2DRsUVG7DR-1GhLmmypQSUFxDQ130_assertion type Assertion NP916729.RAAUsGKV8744Ute8dVU2DRsUVG7DR-1GhLmmypQSUFxDQ130_head.
- 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.