Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP584262.RAo8Nsme7dU3hi3YFCljX2_Kf_eHDUuI8B6aXSmScxFTk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP584262.RAo8Nsme7dU3hi3YFCljX2_Kf_eHDUuI8B6aXSmScxFTk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584262.RAo8Nsme7dU3hi3YFCljX2_Kf_eHDUuI8B6aXSmScxFTk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584262.RAo8Nsme7dU3hi3YFCljX2_Kf_eHDUuI8B6aXSmScxFTk130_provenance.
- NP584262.RAo8Nsme7dU3hi3YFCljX2_Kf_eHDUuI8B6aXSmScxFTk130_assertion description "[A defect in the beta-subunit of the cGMP PDE gene has been shown recently to be the cause for the retinal degeneration in the rd mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584262.RAo8Nsme7dU3hi3YFCljX2_Kf_eHDUuI8B6aXSmScxFTk130_provenance.
- NP584262.RAo8Nsme7dU3hi3YFCljX2_Kf_eHDUuI8B6aXSmScxFTk130_assertion evidence source_evidence_literature NP584262.RAo8Nsme7dU3hi3YFCljX2_Kf_eHDUuI8B6aXSmScxFTk130_provenance.
- NP584262.RAo8Nsme7dU3hi3YFCljX2_Kf_eHDUuI8B6aXSmScxFTk130_assertion SIO_000772 1720239 NP584262.RAo8Nsme7dU3hi3YFCljX2_Kf_eHDUuI8B6aXSmScxFTk130_provenance.
- NP584262.RAo8Nsme7dU3hi3YFCljX2_Kf_eHDUuI8B6aXSmScxFTk130_assertion wasDerivedFrom befree-20140225 NP584262.RAo8Nsme7dU3hi3YFCljX2_Kf_eHDUuI8B6aXSmScxFTk130_provenance.
- NP584262.RAo8Nsme7dU3hi3YFCljX2_Kf_eHDUuI8B6aXSmScxFTk130_assertion wasGeneratedBy ECO_0000203 NP584262.RAo8Nsme7dU3hi3YFCljX2_Kf_eHDUuI8B6aXSmScxFTk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP584262.RAo8Nsme7dU3hi3YFCljX2_Kf_eHDUuI8B6aXSmScxFTk130_provenance.