Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1307179.RAFPBCjVGrMr7XVBMRKal4Z_TXvwNIVp2dPOAewSSbc4w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1307179.RAFPBCjVGrMr7XVBMRKal4Z_TXvwNIVp2dPOAewSSbc4w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1307179.RAFPBCjVGrMr7XVBMRKal4Z_TXvwNIVp2dPOAewSSbc4w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1307179.RAFPBCjVGrMr7XVBMRKal4Z_TXvwNIVp2dPOAewSSbc4w130_provenance.
- NP1307179.RAFPBCjVGrMr7XVBMRKal4Z_TXvwNIVp2dPOAewSSbc4w130_assertion description "[A cloned DNA sequence, RC8, from the short arm of the X chromosome which is linked to the Duchenne muscular dystrophy (DMD) gene has been employed to study linkage relationships with the Xg-linked retinoschisis (RS) locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1307179.RAFPBCjVGrMr7XVBMRKal4Z_TXvwNIVp2dPOAewSSbc4w130_provenance.
- NP1307179.RAFPBCjVGrMr7XVBMRKal4Z_TXvwNIVp2dPOAewSSbc4w130_assertion evidence source_evidence_literature NP1307179.RAFPBCjVGrMr7XVBMRKal4Z_TXvwNIVp2dPOAewSSbc4w130_provenance.
- NP1307179.RAFPBCjVGrMr7XVBMRKal4Z_TXvwNIVp2dPOAewSSbc4w130_assertion SIO_000772 6885047 NP1307179.RAFPBCjVGrMr7XVBMRKal4Z_TXvwNIVp2dPOAewSSbc4w130_provenance.
- NP1307179.RAFPBCjVGrMr7XVBMRKal4Z_TXvwNIVp2dPOAewSSbc4w130_assertion wasDerivedFrom befree-2016 NP1307179.RAFPBCjVGrMr7XVBMRKal4Z_TXvwNIVp2dPOAewSSbc4w130_provenance.
- NP1307179.RAFPBCjVGrMr7XVBMRKal4Z_TXvwNIVp2dPOAewSSbc4w130_assertion wasGeneratedBy ECO_0000203 NP1307179.RAFPBCjVGrMr7XVBMRKal4Z_TXvwNIVp2dPOAewSSbc4w130_provenance.
- befree-2016 importedOn "2016-02-19" NP1307179.RAFPBCjVGrMr7XVBMRKal4Z_TXvwNIVp2dPOAewSSbc4w130_provenance.