Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP668580.RAr4jEabhm5-dc8i2g2VFG6ll7UjAE3dI_0DJmVuuPS_Q130_assertion> ?p ?o ?g. }
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- NP668580.RAr4jEabhm5-dc8i2g2VFG6ll7UjAE3dI_0DJmVuuPS_Q130_assertion type Assertion NP668580.RAr4jEabhm5-dc8i2g2VFG6ll7UjAE3dI_0DJmVuuPS_Q130_head.
- NP668580.RAr4jEabhm5-dc8i2g2VFG6ll7UjAE3dI_0DJmVuuPS_Q130_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." NP668580.RAr4jEabhm5-dc8i2g2VFG6ll7UjAE3dI_0DJmVuuPS_Q130_provenance.
- NP668580.RAr4jEabhm5-dc8i2g2VFG6ll7UjAE3dI_0DJmVuuPS_Q130_assertion evidence source_evidence_literature NP668580.RAr4jEabhm5-dc8i2g2VFG6ll7UjAE3dI_0DJmVuuPS_Q130_provenance.
- NP668580.RAr4jEabhm5-dc8i2g2VFG6ll7UjAE3dI_0DJmVuuPS_Q130_assertion SIO_000772 16916875 NP668580.RAr4jEabhm5-dc8i2g2VFG6ll7UjAE3dI_0DJmVuuPS_Q130_provenance.
- NP668580.RAr4jEabhm5-dc8i2g2VFG6ll7UjAE3dI_0DJmVuuPS_Q130_assertion wasDerivedFrom befree-20150227 NP668580.RAr4jEabhm5-dc8i2g2VFG6ll7UjAE3dI_0DJmVuuPS_Q130_provenance.
- NP668580.RAr4jEabhm5-dc8i2g2VFG6ll7UjAE3dI_0DJmVuuPS_Q130_assertion wasGeneratedBy ECO_0000203 NP668580.RAr4jEabhm5-dc8i2g2VFG6ll7UjAE3dI_0DJmVuuPS_Q130_provenance.