Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_assertion> ?p ?o ?g. }
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- NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_assertion type Assertion NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_head.
- NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_assertion wasGeneratedBy ECO_0000203 NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_provenance.
- NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_assertion wasDerivedFrom befree-20140225 NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_provenance.
- NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_assertion SIO_000772 10973248 NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_provenance.
- NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_assertion evidence source_evidence_literature NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_provenance.
- NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_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." NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_provenance.