Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP643610.RAAQT09stAPna0RQhcVrq3ZpxEbx1i5GNyFWuYVf-eN2U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP643610.RAAQT09stAPna0RQhcVrq3ZpxEbx1i5GNyFWuYVf-eN2U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP643610.RAAQT09stAPna0RQhcVrq3ZpxEbx1i5GNyFWuYVf-eN2U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP643610.RAAQT09stAPna0RQhcVrq3ZpxEbx1i5GNyFWuYVf-eN2U130_provenance.
- NP643610.RAAQT09stAPna0RQhcVrq3ZpxEbx1i5GNyFWuYVf-eN2U130_assertion description "[Myotonic dystrophy type 1 (DM1) is an autosomal-dominant muscular dystrophy caused by expansion of cytosine-thymine-guanine (CTG) trinucleotide repeats in the myotonic dystrophy protein kinase (DMPK) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP643610.RAAQT09stAPna0RQhcVrq3ZpxEbx1i5GNyFWuYVf-eN2U130_provenance.
- NP643610.RAAQT09stAPna0RQhcVrq3ZpxEbx1i5GNyFWuYVf-eN2U130_assertion evidence source_evidence_literature NP643610.RAAQT09stAPna0RQhcVrq3ZpxEbx1i5GNyFWuYVf-eN2U130_provenance.
- NP643610.RAAQT09stAPna0RQhcVrq3ZpxEbx1i5GNyFWuYVf-eN2U130_assertion SIO_000772 19127114 NP643610.RAAQT09stAPna0RQhcVrq3ZpxEbx1i5GNyFWuYVf-eN2U130_provenance.
- NP643610.RAAQT09stAPna0RQhcVrq3ZpxEbx1i5GNyFWuYVf-eN2U130_assertion wasDerivedFrom befree-20140225 NP643610.RAAQT09stAPna0RQhcVrq3ZpxEbx1i5GNyFWuYVf-eN2U130_provenance.
- NP643610.RAAQT09stAPna0RQhcVrq3ZpxEbx1i5GNyFWuYVf-eN2U130_assertion wasGeneratedBy ECO_0000203 NP643610.RAAQT09stAPna0RQhcVrq3ZpxEbx1i5GNyFWuYVf-eN2U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP643610.RAAQT09stAPna0RQhcVrq3ZpxEbx1i5GNyFWuYVf-eN2U130_provenance.