Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP897790.RAdIyftOR8S0mHjMl_yYpdUDqW659XMDAV1_cP2aQ9E2k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP897790.RAdIyftOR8S0mHjMl_yYpdUDqW659XMDAV1_cP2aQ9E2k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP897790.RAdIyftOR8S0mHjMl_yYpdUDqW659XMDAV1_cP2aQ9E2k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP897790.RAdIyftOR8S0mHjMl_yYpdUDqW659XMDAV1_cP2aQ9E2k130_provenance.
- NP897790.RAdIyftOR8S0mHjMl_yYpdUDqW659XMDAV1_cP2aQ9E2k130_assertion wasGeneratedBy ECO_0000203 NP897790.RAdIyftOR8S0mHjMl_yYpdUDqW659XMDAV1_cP2aQ9E2k130_provenance.
- NP897790.RAdIyftOR8S0mHjMl_yYpdUDqW659XMDAV1_cP2aQ9E2k130_assertion wasDerivedFrom befree-20140225 NP897790.RAdIyftOR8S0mHjMl_yYpdUDqW659XMDAV1_cP2aQ9E2k130_provenance.
- NP897790.RAdIyftOR8S0mHjMl_yYpdUDqW659XMDAV1_cP2aQ9E2k130_assertion SIO_000772 23144630 NP897790.RAdIyftOR8S0mHjMl_yYpdUDqW659XMDAV1_cP2aQ9E2k130_provenance.
- NP897790.RAdIyftOR8S0mHjMl_yYpdUDqW659XMDAV1_cP2aQ9E2k130_assertion evidence source_evidence_literature NP897790.RAdIyftOR8S0mHjMl_yYpdUDqW659XMDAV1_cP2aQ9E2k130_provenance.
- NP897790.RAdIyftOR8S0mHjMl_yYpdUDqW659XMDAV1_cP2aQ9E2k130_assertion description "[In asymptomatic carriers CNOT3 is expressed at low levels, allowing higher amounts of wild-type PRPF31 transcripts to be produced and preventing manifestation of retinal degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP897790.RAdIyftOR8S0mHjMl_yYpdUDqW659XMDAV1_cP2aQ9E2k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP897790.RAdIyftOR8S0mHjMl_yYpdUDqW659XMDAV1_cP2aQ9E2k130_provenance.