Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP283766.RAJUGXOt0UC1CUknsCE67kRdKWHmTK52t1pM-DIm5MXNY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP283766.RAJUGXOt0UC1CUknsCE67kRdKWHmTK52t1pM-DIm5MXNY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP283766.RAJUGXOt0UC1CUknsCE67kRdKWHmTK52t1pM-DIm5MXNY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP283766.RAJUGXOt0UC1CUknsCE67kRdKWHmTK52t1pM-DIm5MXNY130_provenance.
- NP283766.RAJUGXOt0UC1CUknsCE67kRdKWHmTK52t1pM-DIm5MXNY130_assertion description "[Sequence variants in a gene coding for a retina-specific ATP-binding cassette (ABCA4) transporter protein, which is responsible for a phenotypically similar Mendelian form of retinal disease, were proposed to increase the risk of ARM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP283766.RAJUGXOt0UC1CUknsCE67kRdKWHmTK52t1pM-DIm5MXNY130_provenance.
- NP283766.RAJUGXOt0UC1CUknsCE67kRdKWHmTK52t1pM-DIm5MXNY130_assertion evidence source_evidence_literature NP283766.RAJUGXOt0UC1CUknsCE67kRdKWHmTK52t1pM-DIm5MXNY130_provenance.
- NP283766.RAJUGXOt0UC1CUknsCE67kRdKWHmTK52t1pM-DIm5MXNY130_assertion SIO_000772 12824224 NP283766.RAJUGXOt0UC1CUknsCE67kRdKWHmTK52t1pM-DIm5MXNY130_provenance.
- NP283766.RAJUGXOt0UC1CUknsCE67kRdKWHmTK52t1pM-DIm5MXNY130_assertion wasDerivedFrom befree-20140225 NP283766.RAJUGXOt0UC1CUknsCE67kRdKWHmTK52t1pM-DIm5MXNY130_provenance.
- NP283766.RAJUGXOt0UC1CUknsCE67kRdKWHmTK52t1pM-DIm5MXNY130_assertion wasGeneratedBy ECO_0000203 NP283766.RAJUGXOt0UC1CUknsCE67kRdKWHmTK52t1pM-DIm5MXNY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP283766.RAJUGXOt0UC1CUknsCE67kRdKWHmTK52t1pM-DIm5MXNY130_provenance.