Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_assertion> ?p ?o ?g. }
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- NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_assertion type Assertion NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_head.
- NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_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." NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_provenance.
- NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_assertion evidence source_evidence_literature NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_provenance.
- NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_assertion SIO_000772 9719369 NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_provenance.
- NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_assertion wasDerivedFrom befree-20140225 NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_provenance.
- NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_assertion wasGeneratedBy ECO_0000203 NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_provenance.