Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_provenance.
- NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_assertion description "[Myotonic dystrophy (DM), the most common inherited muscle disorder, is caused by a CTG expansion in the 3`-untranslated region of a protein kinase gene ( DMPK ).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_provenance.
- NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_assertion evidence source_evidence_literature NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_provenance.
- NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_assertion SIO_000772 10332033 NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_provenance.
- NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_assertion wasDerivedFrom befree-20140225 NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_provenance.
- NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_assertion wasGeneratedBy ECO_0000203 NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_provenance.