Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP293150.RAxsAb4l0g2Gg1ZVzZ1jAIaNHH2pkpPOrDqmkCyUsdc-Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP293150.RAxsAb4l0g2Gg1ZVzZ1jAIaNHH2pkpPOrDqmkCyUsdc-Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP293150.RAxsAb4l0g2Gg1ZVzZ1jAIaNHH2pkpPOrDqmkCyUsdc-Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP293150.RAxsAb4l0g2Gg1ZVzZ1jAIaNHH2pkpPOrDqmkCyUsdc-Q130_provenance.
- NP293150.RAxsAb4l0g2Gg1ZVzZ1jAIaNHH2pkpPOrDqmkCyUsdc-Q130_assertion description "[Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP293150.RAxsAb4l0g2Gg1ZVzZ1jAIaNHH2pkpPOrDqmkCyUsdc-Q130_provenance.
- NP293150.RAxsAb4l0g2Gg1ZVzZ1jAIaNHH2pkpPOrDqmkCyUsdc-Q130_assertion evidence source_evidence_literature NP293150.RAxsAb4l0g2Gg1ZVzZ1jAIaNHH2pkpPOrDqmkCyUsdc-Q130_provenance.
- NP293150.RAxsAb4l0g2Gg1ZVzZ1jAIaNHH2pkpPOrDqmkCyUsdc-Q130_assertion SIO_000772 10958761 NP293150.RAxsAb4l0g2Gg1ZVzZ1jAIaNHH2pkpPOrDqmkCyUsdc-Q130_provenance.
- NP293150.RAxsAb4l0g2Gg1ZVzZ1jAIaNHH2pkpPOrDqmkCyUsdc-Q130_assertion wasDerivedFrom befree-2016 NP293150.RAxsAb4l0g2Gg1ZVzZ1jAIaNHH2pkpPOrDqmkCyUsdc-Q130_provenance.
- NP293150.RAxsAb4l0g2Gg1ZVzZ1jAIaNHH2pkpPOrDqmkCyUsdc-Q130_assertion wasGeneratedBy ECO_0000203 NP293150.RAxsAb4l0g2Gg1ZVzZ1jAIaNHH2pkpPOrDqmkCyUsdc-Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP293150.RAxsAb4l0g2Gg1ZVzZ1jAIaNHH2pkpPOrDqmkCyUsdc-Q130_provenance.