Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP333338.RAurXcUY9K3efXcilu6-pKmjZSC3sYOTWnIJeOqg5pKFk130_assertion> ?p ?o ?g. }
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- NP333338.RAurXcUY9K3efXcilu6-pKmjZSC3sYOTWnIJeOqg5pKFk130_assertion type Assertion NP333338.RAurXcUY9K3efXcilu6-pKmjZSC3sYOTWnIJeOqg5pKFk130_head.
- NP333338.RAurXcUY9K3efXcilu6-pKmjZSC3sYOTWnIJeOqg5pKFk130_assertion description "[More than 20 mutations in the GJB2 gene are associated with DFNB1, a prevalent type of autosomal recessive non-syndromic neurosensory deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333338.RAurXcUY9K3efXcilu6-pKmjZSC3sYOTWnIJeOqg5pKFk130_provenance.
- NP333338.RAurXcUY9K3efXcilu6-pKmjZSC3sYOTWnIJeOqg5pKFk130_assertion evidence source_evidence_literature NP333338.RAurXcUY9K3efXcilu6-pKmjZSC3sYOTWnIJeOqg5pKFk130_provenance.
- NP333338.RAurXcUY9K3efXcilu6-pKmjZSC3sYOTWnIJeOqg5pKFk130_assertion SIO_000772 11603757 NP333338.RAurXcUY9K3efXcilu6-pKmjZSC3sYOTWnIJeOqg5pKFk130_provenance.
- NP333338.RAurXcUY9K3efXcilu6-pKmjZSC3sYOTWnIJeOqg5pKFk130_assertion wasDerivedFrom befree-2016 NP333338.RAurXcUY9K3efXcilu6-pKmjZSC3sYOTWnIJeOqg5pKFk130_provenance.
- NP333338.RAurXcUY9K3efXcilu6-pKmjZSC3sYOTWnIJeOqg5pKFk130_assertion wasGeneratedBy ECO_0000203 NP333338.RAurXcUY9K3efXcilu6-pKmjZSC3sYOTWnIJeOqg5pKFk130_provenance.