Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP450491.RAZa7Hqjc6nG0TVJvG-Bp5CnvVfANtRmm3acl_NTU8e6w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP450491.RAZa7Hqjc6nG0TVJvG-Bp5CnvVfANtRmm3acl_NTU8e6w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP450491.RAZa7Hqjc6nG0TVJvG-Bp5CnvVfANtRmm3acl_NTU8e6w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP450491.RAZa7Hqjc6nG0TVJvG-Bp5CnvVfANtRmm3acl_NTU8e6w130_provenance.
- NP450491.RAZa7Hqjc6nG0TVJvG-Bp5CnvVfANtRmm3acl_NTU8e6w130_assertion description "[Our data provide evidence that mutations in this gene, designated RP2, are responsible for progressive retinal degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450491.RAZa7Hqjc6nG0TVJvG-Bp5CnvVfANtRmm3acl_NTU8e6w130_provenance.
- NP450491.RAZa7Hqjc6nG0TVJvG-Bp5CnvVfANtRmm3acl_NTU8e6w130_assertion evidence source_evidence_literature NP450491.RAZa7Hqjc6nG0TVJvG-Bp5CnvVfANtRmm3acl_NTU8e6w130_provenance.
- NP450491.RAZa7Hqjc6nG0TVJvG-Bp5CnvVfANtRmm3acl_NTU8e6w130_assertion SIO_000772 9697692 NP450491.RAZa7Hqjc6nG0TVJvG-Bp5CnvVfANtRmm3acl_NTU8e6w130_provenance.
- NP450491.RAZa7Hqjc6nG0TVJvG-Bp5CnvVfANtRmm3acl_NTU8e6w130_assertion wasDerivedFrom befree-20140225 NP450491.RAZa7Hqjc6nG0TVJvG-Bp5CnvVfANtRmm3acl_NTU8e6w130_provenance.
- NP450491.RAZa7Hqjc6nG0TVJvG-Bp5CnvVfANtRmm3acl_NTU8e6w130_assertion wasGeneratedBy ECO_0000203 NP450491.RAZa7Hqjc6nG0TVJvG-Bp5CnvVfANtRmm3acl_NTU8e6w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP450491.RAZa7Hqjc6nG0TVJvG-Bp5CnvVfANtRmm3acl_NTU8e6w130_provenance.