Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1329902.RAnc7cJgn8XMDiA5GNGFtT1SlY9n3R94cW8A_48ZImdWs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1329902.RAnc7cJgn8XMDiA5GNGFtT1SlY9n3R94cW8A_48ZImdWs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1329902.RAnc7cJgn8XMDiA5GNGFtT1SlY9n3R94cW8A_48ZImdWs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1329902.RAnc7cJgn8XMDiA5GNGFtT1SlY9n3R94cW8A_48ZImdWs130_provenance.
- NP1329902.RAnc7cJgn8XMDiA5GNGFtT1SlY9n3R94cW8A_48ZImdWs130_assertion description "[Using highly informative microsatellite DNA markers in eight multiplex families, we were able to exclude Stargardt's disease from the vicinity of the CLN1 and CLN3 loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1329902.RAnc7cJgn8XMDiA5GNGFtT1SlY9n3R94cW8A_48ZImdWs130_provenance.
- NP1329902.RAnc7cJgn8XMDiA5GNGFtT1SlY9n3R94cW8A_48ZImdWs130_assertion evidence source_evidence_literature NP1329902.RAnc7cJgn8XMDiA5GNGFtT1SlY9n3R94cW8A_48ZImdWs130_provenance.
- NP1329902.RAnc7cJgn8XMDiA5GNGFtT1SlY9n3R94cW8A_48ZImdWs130_assertion SIO_000772 8014971 NP1329902.RAnc7cJgn8XMDiA5GNGFtT1SlY9n3R94cW8A_48ZImdWs130_provenance.
- NP1329902.RAnc7cJgn8XMDiA5GNGFtT1SlY9n3R94cW8A_48ZImdWs130_assertion wasDerivedFrom befree-2016 NP1329902.RAnc7cJgn8XMDiA5GNGFtT1SlY9n3R94cW8A_48ZImdWs130_provenance.
- NP1329902.RAnc7cJgn8XMDiA5GNGFtT1SlY9n3R94cW8A_48ZImdWs130_assertion wasGeneratedBy ECO_0000203 NP1329902.RAnc7cJgn8XMDiA5GNGFtT1SlY9n3R94cW8A_48ZImdWs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1329902.RAnc7cJgn8XMDiA5GNGFtT1SlY9n3R94cW8A_48ZImdWs130_provenance.