Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP480361.RAlxFS2zpezuF1L7-Iet42ZZ4zfUOQZz-Kc-nrA34tm2U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP480361.RAlxFS2zpezuF1L7-Iet42ZZ4zfUOQZz-Kc-nrA34tm2U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP480361.RAlxFS2zpezuF1L7-Iet42ZZ4zfUOQZz-Kc-nrA34tm2U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP480361.RAlxFS2zpezuF1L7-Iet42ZZ4zfUOQZz-Kc-nrA34tm2U130_provenance.
- NP480361.RAlxFS2zpezuF1L7-Iet42ZZ4zfUOQZz-Kc-nrA34tm2U130_assertion description "[Genetic studies excluded mutations in the DM type 1 (DM1) gene, but revealed a CCTG repeat expansion in the ZNF9 gene, which is associated with DM2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480361.RAlxFS2zpezuF1L7-Iet42ZZ4zfUOQZz-Kc-nrA34tm2U130_provenance.
- NP480361.RAlxFS2zpezuF1L7-Iet42ZZ4zfUOQZz-Kc-nrA34tm2U130_assertion evidence source_evidence_literature NP480361.RAlxFS2zpezuF1L7-Iet42ZZ4zfUOQZz-Kc-nrA34tm2U130_provenance.
- NP480361.RAlxFS2zpezuF1L7-Iet42ZZ4zfUOQZz-Kc-nrA34tm2U130_assertion SIO_000772 15704146 NP480361.RAlxFS2zpezuF1L7-Iet42ZZ4zfUOQZz-Kc-nrA34tm2U130_provenance.
- NP480361.RAlxFS2zpezuF1L7-Iet42ZZ4zfUOQZz-Kc-nrA34tm2U130_assertion wasDerivedFrom befree-2016 NP480361.RAlxFS2zpezuF1L7-Iet42ZZ4zfUOQZz-Kc-nrA34tm2U130_provenance.
- NP480361.RAlxFS2zpezuF1L7-Iet42ZZ4zfUOQZz-Kc-nrA34tm2U130_assertion wasGeneratedBy ECO_0000203 NP480361.RAlxFS2zpezuF1L7-Iet42ZZ4zfUOQZz-Kc-nrA34tm2U130_provenance.
- befree-2016 importedOn "2016-02-19" NP480361.RAlxFS2zpezuF1L7-Iet42ZZ4zfUOQZz-Kc-nrA34tm2U130_provenance.