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- source_evidence_literature type ECO_0000212 NP587045.RA5_1AkHbdT_kTegzY-ICo9ZuKU12vw_biEnew_6hIoxI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP587045.RA5_1AkHbdT_kTegzY-ICo9ZuKU12vw_biEnew_6hIoxI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP587045.RA5_1AkHbdT_kTegzY-ICo9ZuKU12vw_biEnew_6hIoxI130_provenance.
- NP587045.RA5_1AkHbdT_kTegzY-ICo9ZuKU12vw_biEnew_6hIoxI130_assertion description "[In this article we review these mutations and describe the consequences of specific mutations on GCAP1 structure and GC stimulation.We discuss the heterogeneity of autosomal dominant cone and cone-rod dystrophies (adCD, and adCORD, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587045.RA5_1AkHbdT_kTegzY-ICo9ZuKU12vw_biEnew_6hIoxI130_provenance.
- NP587045.RA5_1AkHbdT_kTegzY-ICo9ZuKU12vw_biEnew_6hIoxI130_assertion evidence source_evidence_literature NP587045.RA5_1AkHbdT_kTegzY-ICo9ZuKU12vw_biEnew_6hIoxI130_provenance.
- NP587045.RA5_1AkHbdT_kTegzY-ICo9ZuKU12vw_biEnew_6hIoxI130_assertion SIO_000772 20238026 NP587045.RA5_1AkHbdT_kTegzY-ICo9ZuKU12vw_biEnew_6hIoxI130_provenance.
- NP587045.RA5_1AkHbdT_kTegzY-ICo9ZuKU12vw_biEnew_6hIoxI130_assertion wasDerivedFrom befree-20140225 NP587045.RA5_1AkHbdT_kTegzY-ICo9ZuKU12vw_biEnew_6hIoxI130_provenance.
- NP587045.RA5_1AkHbdT_kTegzY-ICo9ZuKU12vw_biEnew_6hIoxI130_assertion wasGeneratedBy ECO_0000203 NP587045.RA5_1AkHbdT_kTegzY-ICo9ZuKU12vw_biEnew_6hIoxI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP587045.RA5_1AkHbdT_kTegzY-ICo9ZuKU12vw_biEnew_6hIoxI130_provenance.