Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP361490.RADj2I4wEFtKyOGuFFyMMGxfTA2MmBVKy-R2VXIIVrDwI130_assertion> ?p ?o ?g. }
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- NP361490.RADj2I4wEFtKyOGuFFyMMGxfTA2MmBVKy-R2VXIIVrDwI130_assertion type Assertion NP361490.RADj2I4wEFtKyOGuFFyMMGxfTA2MmBVKy-R2VXIIVrDwI130_head.
- NP361490.RADj2I4wEFtKyOGuFFyMMGxfTA2MmBVKy-R2VXIIVrDwI130_assertion description "[Mutations in the Connexin 26 (Cx26) gene have been found to account for approximately 20% of all childhood deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP361490.RADj2I4wEFtKyOGuFFyMMGxfTA2MmBVKy-R2VXIIVrDwI130_provenance.
- NP361490.RADj2I4wEFtKyOGuFFyMMGxfTA2MmBVKy-R2VXIIVrDwI130_assertion evidence source_evidence_literature NP361490.RADj2I4wEFtKyOGuFFyMMGxfTA2MmBVKy-R2VXIIVrDwI130_provenance.
- NP361490.RADj2I4wEFtKyOGuFFyMMGxfTA2MmBVKy-R2VXIIVrDwI130_assertion SIO_000772 12121355 NP361490.RADj2I4wEFtKyOGuFFyMMGxfTA2MmBVKy-R2VXIIVrDwI130_provenance.
- NP361490.RADj2I4wEFtKyOGuFFyMMGxfTA2MmBVKy-R2VXIIVrDwI130_assertion wasDerivedFrom befree-2016 NP361490.RADj2I4wEFtKyOGuFFyMMGxfTA2MmBVKy-R2VXIIVrDwI130_provenance.
- NP361490.RADj2I4wEFtKyOGuFFyMMGxfTA2MmBVKy-R2VXIIVrDwI130_assertion wasGeneratedBy ECO_0000203 NP361490.RADj2I4wEFtKyOGuFFyMMGxfTA2MmBVKy-R2VXIIVrDwI130_provenance.