Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP319278.RAATka8XGFERzObwnX9sofaGcML7H2Ufi7ONfCMIBA2Yc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP319278.RAATka8XGFERzObwnX9sofaGcML7H2Ufi7ONfCMIBA2Yc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP319278.RAATka8XGFERzObwnX9sofaGcML7H2Ufi7ONfCMIBA2Yc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP319278.RAATka8XGFERzObwnX9sofaGcML7H2Ufi7ONfCMIBA2Yc130_provenance.
- NP319278.RAATka8XGFERzObwnX9sofaGcML7H2Ufi7ONfCMIBA2Yc130_assertion description "[Based on recent studies of the photoreceptor-specific ABC transporter gene ABCR (ABCA4) in Stargardt disease (STGD1) and other retinal dystrophies, we and others have developed a model in which the severity of retinal disease correlates inversely with residual ABCR activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319278.RAATka8XGFERzObwnX9sofaGcML7H2Ufi7ONfCMIBA2Yc130_provenance.
- NP319278.RAATka8XGFERzObwnX9sofaGcML7H2Ufi7ONfCMIBA2Yc130_assertion evidence source_evidence_literature NP319278.RAATka8XGFERzObwnX9sofaGcML7H2Ufi7ONfCMIBA2Yc130_provenance.
- NP319278.RAATka8XGFERzObwnX9sofaGcML7H2Ufi7ONfCMIBA2Yc130_assertion SIO_000772 11379881 NP319278.RAATka8XGFERzObwnX9sofaGcML7H2Ufi7ONfCMIBA2Yc130_provenance.
- NP319278.RAATka8XGFERzObwnX9sofaGcML7H2Ufi7ONfCMIBA2Yc130_assertion wasDerivedFrom befree-2016 NP319278.RAATka8XGFERzObwnX9sofaGcML7H2Ufi7ONfCMIBA2Yc130_provenance.
- NP319278.RAATka8XGFERzObwnX9sofaGcML7H2Ufi7ONfCMIBA2Yc130_assertion wasGeneratedBy ECO_0000203 NP319278.RAATka8XGFERzObwnX9sofaGcML7H2Ufi7ONfCMIBA2Yc130_provenance.
- befree-2016 importedOn "2016-02-19" NP319278.RAATka8XGFERzObwnX9sofaGcML7H2Ufi7ONfCMIBA2Yc130_provenance.