Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP341253.RANPfyNCdbU5K1BXVPf0MhIMV18jwMFvjCRn1CIXHM49A130_provenance.