Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP836263.RABmfJlBwTLTreZo914gfUGandUJUHnSA1IS7tTFZu-mk130_assertion> ?p ?o ?g. }
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- NP836263.RABmfJlBwTLTreZo914gfUGandUJUHnSA1IS7tTFZu-mk130_assertion type Assertion NP836263.RABmfJlBwTLTreZo914gfUGandUJUHnSA1IS7tTFZu-mk130_head.
- NP836263.RABmfJlBwTLTreZo914gfUGandUJUHnSA1IS7tTFZu-mk130_assertion wasGeneratedBy ECO_0000203 NP836263.RABmfJlBwTLTreZo914gfUGandUJUHnSA1IS7tTFZu-mk130_provenance.
- NP836263.RABmfJlBwTLTreZo914gfUGandUJUHnSA1IS7tTFZu-mk130_assertion wasDerivedFrom befree-20150227 NP836263.RABmfJlBwTLTreZo914gfUGandUJUHnSA1IS7tTFZu-mk130_provenance.
- NP836263.RABmfJlBwTLTreZo914gfUGandUJUHnSA1IS7tTFZu-mk130_assertion SIO_000772 10973248 NP836263.RABmfJlBwTLTreZo914gfUGandUJUHnSA1IS7tTFZu-mk130_provenance.
- NP836263.RABmfJlBwTLTreZo914gfUGandUJUHnSA1IS7tTFZu-mk130_assertion evidence source_evidence_literature NP836263.RABmfJlBwTLTreZo914gfUGandUJUHnSA1IS7tTFZu-mk130_provenance.
- NP836263.RABmfJlBwTLTreZo914gfUGandUJUHnSA1IS7tTFZu-mk130_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." NP836263.RABmfJlBwTLTreZo914gfUGandUJUHnSA1IS7tTFZu-mk130_provenance.