Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615913.RA0PSug8mCnwPeXbAs6ST8s8tSNQJVvOecNkI0Cx5Wycw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615913.RA0PSug8mCnwPeXbAs6ST8s8tSNQJVvOecNkI0Cx5Wycw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615913.RA0PSug8mCnwPeXbAs6ST8s8tSNQJVvOecNkI0Cx5Wycw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615913.RA0PSug8mCnwPeXbAs6ST8s8tSNQJVvOecNkI0Cx5Wycw130_provenance.
- NP615913.RA0PSug8mCnwPeXbAs6ST8s8tSNQJVvOecNkI0Cx5Wycw130_assertion description "[Myotonic dystrophy type 1 (DM1) is caused by expansion of a CTG triplet repeat in the 3' untranslated region of the DMPK gene that encodes a serine-threonine kinase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615913.RA0PSug8mCnwPeXbAs6ST8s8tSNQJVvOecNkI0Cx5Wycw130_provenance.
- NP615913.RA0PSug8mCnwPeXbAs6ST8s8tSNQJVvOecNkI0Cx5Wycw130_assertion evidence source_evidence_literature NP615913.RA0PSug8mCnwPeXbAs6ST8s8tSNQJVvOecNkI0Cx5Wycw130_provenance.
- NP615913.RA0PSug8mCnwPeXbAs6ST8s8tSNQJVvOecNkI0Cx5Wycw130_assertion SIO_000772 23680132 NP615913.RA0PSug8mCnwPeXbAs6ST8s8tSNQJVvOecNkI0Cx5Wycw130_provenance.
- NP615913.RA0PSug8mCnwPeXbAs6ST8s8tSNQJVvOecNkI0Cx5Wycw130_assertion wasDerivedFrom befree-20140225 NP615913.RA0PSug8mCnwPeXbAs6ST8s8tSNQJVvOecNkI0Cx5Wycw130_provenance.
- NP615913.RA0PSug8mCnwPeXbAs6ST8s8tSNQJVvOecNkI0Cx5Wycw130_assertion wasGeneratedBy ECO_0000203 NP615913.RA0PSug8mCnwPeXbAs6ST8s8tSNQJVvOecNkI0Cx5Wycw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615913.RA0PSug8mCnwPeXbAs6ST8s8tSNQJVvOecNkI0Cx5Wycw130_provenance.