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- source_evidence_literature type ECO_0000212 NP1384919.RAdfpQqlB97Rax1--UWCnQH-pjkAve6B5aj-HSolzh_h0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1384919.RAdfpQqlB97Rax1--UWCnQH-pjkAve6B5aj-HSolzh_h0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1384919.RAdfpQqlB97Rax1--UWCnQH-pjkAve6B5aj-HSolzh_h0130_provenance.
- NP1384919.RAdfpQqlB97Rax1--UWCnQH-pjkAve6B5aj-HSolzh_h0130_assertion description "[Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1384919.RAdfpQqlB97Rax1--UWCnQH-pjkAve6B5aj-HSolzh_h0130_provenance.
- NP1384919.RAdfpQqlB97Rax1--UWCnQH-pjkAve6B5aj-HSolzh_h0130_assertion evidence source_evidence_literature NP1384919.RAdfpQqlB97Rax1--UWCnQH-pjkAve6B5aj-HSolzh_h0130_provenance.
- NP1384919.RAdfpQqlB97Rax1--UWCnQH-pjkAve6B5aj-HSolzh_h0130_assertion SIO_000772 9390563 NP1384919.RAdfpQqlB97Rax1--UWCnQH-pjkAve6B5aj-HSolzh_h0130_provenance.
- NP1384919.RAdfpQqlB97Rax1--UWCnQH-pjkAve6B5aj-HSolzh_h0130_assertion wasDerivedFrom befree-2016 NP1384919.RAdfpQqlB97Rax1--UWCnQH-pjkAve6B5aj-HSolzh_h0130_provenance.
- NP1384919.RAdfpQqlB97Rax1--UWCnQH-pjkAve6B5aj-HSolzh_h0130_assertion wasGeneratedBy ECO_0000203 NP1384919.RAdfpQqlB97Rax1--UWCnQH-pjkAve6B5aj-HSolzh_h0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1384919.RAdfpQqlB97Rax1--UWCnQH-pjkAve6B5aj-HSolzh_h0130_provenance.