Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP668566.RAYL-ASIpJ64DifA7Z-C1qlwEVvNkKlLvtFDDHpTjERAw130_assertion> ?p ?o ?g. }
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- NP668566.RAYL-ASIpJ64DifA7Z-C1qlwEVvNkKlLvtFDDHpTjERAw130_assertion type Assertion NP668566.RAYL-ASIpJ64DifA7Z-C1qlwEVvNkKlLvtFDDHpTjERAw130_head.
- NP668566.RAYL-ASIpJ64DifA7Z-C1qlwEVvNkKlLvtFDDHpTjERAw130_assertion description "[To identify suspected RDS mutations in families in which different people have been identified with either generalised retinal dystrophy or macular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668566.RAYL-ASIpJ64DifA7Z-C1qlwEVvNkKlLvtFDDHpTjERAw130_provenance.
- NP668566.RAYL-ASIpJ64DifA7Z-C1qlwEVvNkKlLvtFDDHpTjERAw130_assertion evidence source_evidence_literature NP668566.RAYL-ASIpJ64DifA7Z-C1qlwEVvNkKlLvtFDDHpTjERAw130_provenance.
- NP668566.RAYL-ASIpJ64DifA7Z-C1qlwEVvNkKlLvtFDDHpTjERAw130_assertion SIO_000772 16916875 NP668566.RAYL-ASIpJ64DifA7Z-C1qlwEVvNkKlLvtFDDHpTjERAw130_provenance.
- NP668566.RAYL-ASIpJ64DifA7Z-C1qlwEVvNkKlLvtFDDHpTjERAw130_assertion wasDerivedFrom befree-20150227 NP668566.RAYL-ASIpJ64DifA7Z-C1qlwEVvNkKlLvtFDDHpTjERAw130_provenance.
- NP668566.RAYL-ASIpJ64DifA7Z-C1qlwEVvNkKlLvtFDDHpTjERAw130_assertion wasGeneratedBy ECO_0000203 NP668566.RAYL-ASIpJ64DifA7Z-C1qlwEVvNkKlLvtFDDHpTjERAw130_provenance.