Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_assertion> ?p ?o ?g. }
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- NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_assertion type Assertion NP614562.RAv3vHpoIuT85kiwtaC0wpRngC2ABwh3ZxICw3xHYH6iE130_head.
- 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.