Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP713993.RAFUSG-LGPjkpJ51lzA2V7fHfXKlqXbpGvLThU_E5Wemc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP713993.RAFUSG-LGPjkpJ51lzA2V7fHfXKlqXbpGvLThU_E5Wemc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP713993.RAFUSG-LGPjkpJ51lzA2V7fHfXKlqXbpGvLThU_E5Wemc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP713993.RAFUSG-LGPjkpJ51lzA2V7fHfXKlqXbpGvLThU_E5Wemc130_provenance.
- NP713993.RAFUSG-LGPjkpJ51lzA2V7fHfXKlqXbpGvLThU_E5Wemc130_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." NP713993.RAFUSG-LGPjkpJ51lzA2V7fHfXKlqXbpGvLThU_E5Wemc130_provenance.
- NP713993.RAFUSG-LGPjkpJ51lzA2V7fHfXKlqXbpGvLThU_E5Wemc130_assertion evidence source_evidence_literature NP713993.RAFUSG-LGPjkpJ51lzA2V7fHfXKlqXbpGvLThU_E5Wemc130_provenance.
- NP713993.RAFUSG-LGPjkpJ51lzA2V7fHfXKlqXbpGvLThU_E5Wemc130_assertion SIO_000772 10782214 NP713993.RAFUSG-LGPjkpJ51lzA2V7fHfXKlqXbpGvLThU_E5Wemc130_provenance.
- NP713993.RAFUSG-LGPjkpJ51lzA2V7fHfXKlqXbpGvLThU_E5Wemc130_assertion wasDerivedFrom befree-20140225 NP713993.RAFUSG-LGPjkpJ51lzA2V7fHfXKlqXbpGvLThU_E5Wemc130_provenance.
- NP713993.RAFUSG-LGPjkpJ51lzA2V7fHfXKlqXbpGvLThU_E5Wemc130_assertion wasGeneratedBy ECO_0000203 NP713993.RAFUSG-LGPjkpJ51lzA2V7fHfXKlqXbpGvLThU_E5Wemc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP713993.RAFUSG-LGPjkpJ51lzA2V7fHfXKlqXbpGvLThU_E5Wemc130_provenance.