Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP912266.RAKpb3Awj_v2CAgmQY5FknzzD5i2bEcOsDF1-KnS4W0iY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP912266.RAKpb3Awj_v2CAgmQY5FknzzD5i2bEcOsDF1-KnS4W0iY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP912266.RAKpb3Awj_v2CAgmQY5FknzzD5i2bEcOsDF1-KnS4W0iY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP912266.RAKpb3Awj_v2CAgmQY5FknzzD5i2bEcOsDF1-KnS4W0iY130_provenance.
- NP912266.RAKpb3Awj_v2CAgmQY5FknzzD5i2bEcOsDF1-KnS4W0iY130_assertion wasGeneratedBy ECO_0000203 NP912266.RAKpb3Awj_v2CAgmQY5FknzzD5i2bEcOsDF1-KnS4W0iY130_provenance.
- NP912266.RAKpb3Awj_v2CAgmQY5FknzzD5i2bEcOsDF1-KnS4W0iY130_assertion wasDerivedFrom befree-20140225 NP912266.RAKpb3Awj_v2CAgmQY5FknzzD5i2bEcOsDF1-KnS4W0iY130_provenance.
- NP912266.RAKpb3Awj_v2CAgmQY5FknzzD5i2bEcOsDF1-KnS4W0iY130_assertion SIO_000772 22855823 NP912266.RAKpb3Awj_v2CAgmQY5FknzzD5i2bEcOsDF1-KnS4W0iY130_provenance.
- NP912266.RAKpb3Awj_v2CAgmQY5FknzzD5i2bEcOsDF1-KnS4W0iY130_assertion evidence source_evidence_literature NP912266.RAKpb3Awj_v2CAgmQY5FknzzD5i2bEcOsDF1-KnS4W0iY130_provenance.
- NP912266.RAKpb3Awj_v2CAgmQY5FknzzD5i2bEcOsDF1-KnS4W0iY130_assertion description "[The cause of degeneration in norpA(P24) is the failure to activate CaMKII (Ca(2+)/calmodulin-dependent protein kinase II) and retinal degeneration C (RDGC) because of a loss of light-dependent Ca(2+) entry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP912266.RAKpb3Awj_v2CAgmQY5FknzzD5i2bEcOsDF1-KnS4W0iY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP912266.RAKpb3Awj_v2CAgmQY5FknzzD5i2bEcOsDF1-KnS4W0iY130_provenance.