Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668580.RAr4jEabhm5-dc8i2g2VFG6ll7UjAE3dI_0DJmVuuPS_Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP668580.RAr4jEabhm5-dc8i2g2VFG6ll7UjAE3dI_0DJmVuuPS_Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668580.RAr4jEabhm5-dc8i2g2VFG6ll7UjAE3dI_0DJmVuuPS_Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668580.RAr4jEabhm5-dc8i2g2VFG6ll7UjAE3dI_0DJmVuuPS_Q130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP668580.RAr4jEabhm5-dc8i2g2VFG6ll7UjAE3dI_0DJmVuuPS_Q130_provenance.