Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP478195.RAQ2GvSuuMjkeHL1s3c7MBNabVoJ2gRaRNZjvkqU3HE54130_provenance.