Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_provenance.
- NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_assertion description "[By genetic linkage analysis, several retinal dystrophies including one form of autosomal dominant Stargardt-like macular dystrophy (STGD3), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1) have previously been localised to a region on proximal 6q that overlaps the IMPG1 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_provenance.
- NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_assertion evidence source_evidence_literature NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_provenance.
- NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_assertion SIO_000772 9719369 NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_provenance.
- NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_assertion wasDerivedFrom befree-20140225 NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_provenance.
- NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_assertion wasGeneratedBy ECO_0000203 NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_provenance.