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- source_evidence_literature type ECO_0000212 NP613993.RAuXDOm0DyZpKHlEze5anRBmQWdA_OQ7Ku5fjqRmYvWsI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP613993.RAuXDOm0DyZpKHlEze5anRBmQWdA_OQ7Ku5fjqRmYvWsI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP613993.RAuXDOm0DyZpKHlEze5anRBmQWdA_OQ7Ku5fjqRmYvWsI130_provenance.
- NP613993.RAuXDOm0DyZpKHlEze5anRBmQWdA_OQ7Ku5fjqRmYvWsI130_assertion description "[Mutations in PDE6A and the PDE6B genes lead to autosomal recessive (ar) forms of retinitis pigmentosa (RP) in human and to the homologous disease in dogs, designated generalised progressive retinal atrophy (gPRA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP613993.RAuXDOm0DyZpKHlEze5anRBmQWdA_OQ7Ku5fjqRmYvWsI130_provenance.
- NP613993.RAuXDOm0DyZpKHlEze5anRBmQWdA_OQ7Ku5fjqRmYvWsI130_assertion evidence source_evidence_literature NP613993.RAuXDOm0DyZpKHlEze5anRBmQWdA_OQ7Ku5fjqRmYvWsI130_provenance.
- NP613993.RAuXDOm0DyZpKHlEze5anRBmQWdA_OQ7Ku5fjqRmYvWsI130_assertion SIO_000772 10782214 NP613993.RAuXDOm0DyZpKHlEze5anRBmQWdA_OQ7Ku5fjqRmYvWsI130_provenance.
- NP613993.RAuXDOm0DyZpKHlEze5anRBmQWdA_OQ7Ku5fjqRmYvWsI130_assertion wasDerivedFrom befree-20150227 NP613993.RAuXDOm0DyZpKHlEze5anRBmQWdA_OQ7Ku5fjqRmYvWsI130_provenance.
- NP613993.RAuXDOm0DyZpKHlEze5anRBmQWdA_OQ7Ku5fjqRmYvWsI130_assertion wasGeneratedBy ECO_0000203 NP613993.RAuXDOm0DyZpKHlEze5anRBmQWdA_OQ7Ku5fjqRmYvWsI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP613993.RAuXDOm0DyZpKHlEze5anRBmQWdA_OQ7Ku5fjqRmYvWsI130_provenance.