Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP992864.RATYzgA3g6Kv8Uh_AxX4FAROozpVgSyBIFn18qnBmaSTY#assertion> ?p ?o ?g. }
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- assertion description "[The molecular basis of the disorder is a homozygous 122-kb deletion of 11p14-15, which includes part of ABCC8 and overlaps with the locus for Usher syndrome type 1C and DFNB18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion evidence source_evidence_literature provenance.
- assertion SIO_000772 10973248 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.