Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_provenance.
- NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_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." NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_provenance.
- NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_assertion evidence source_evidence_literature NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_provenance.
- NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_assertion SIO_000772 10782214 NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_provenance.
- NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_assertion wasDerivedFrom befree-20140225 NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_provenance.
- NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_assertion wasGeneratedBy ECO_0000203 NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP602266.RAwGZA_IpCoccV__woxn1MuiGMGjroWGN-5yOB7RVc03k130_provenance.