Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP218974.RAFbIBCqfIm8HqbFryOghOFtIoeo3azGEquwNIonEaYLQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP218974.RAFbIBCqfIm8HqbFryOghOFtIoeo3azGEquwNIonEaYLQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP218974.RAFbIBCqfIm8HqbFryOghOFtIoeo3azGEquwNIonEaYLQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP218974.RAFbIBCqfIm8HqbFryOghOFtIoeo3azGEquwNIonEaYLQ130_provenance.
- NP218974.RAFbIBCqfIm8HqbFryOghOFtIoeo3azGEquwNIonEaYLQ130_assertion description "[Some features of GPS[+] overlap with Stargardt disease (STGD1), a recessive macular dystrophy caused by biallelic sequence variants in the ATP-binding cassette transporter 4 (ABCA4) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218974.RAFbIBCqfIm8HqbFryOghOFtIoeo3azGEquwNIonEaYLQ130_provenance.
- NP218974.RAFbIBCqfIm8HqbFryOghOFtIoeo3azGEquwNIonEaYLQ130_assertion evidence source_evidence_literature NP218974.RAFbIBCqfIm8HqbFryOghOFtIoeo3azGEquwNIonEaYLQ130_provenance.
- NP218974.RAFbIBCqfIm8HqbFryOghOFtIoeo3azGEquwNIonEaYLQ130_assertion SIO_000772 22427542 NP218974.RAFbIBCqfIm8HqbFryOghOFtIoeo3azGEquwNIonEaYLQ130_provenance.
- NP218974.RAFbIBCqfIm8HqbFryOghOFtIoeo3azGEquwNIonEaYLQ130_assertion wasDerivedFrom befree-20150227 NP218974.RAFbIBCqfIm8HqbFryOghOFtIoeo3azGEquwNIonEaYLQ130_provenance.
- NP218974.RAFbIBCqfIm8HqbFryOghOFtIoeo3azGEquwNIonEaYLQ130_assertion wasGeneratedBy ECO_0000203 NP218974.RAFbIBCqfIm8HqbFryOghOFtIoeo3azGEquwNIonEaYLQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP218974.RAFbIBCqfIm8HqbFryOghOFtIoeo3azGEquwNIonEaYLQ130_provenance.