Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP355921.RAW0f8-4luowGrelDuBQw4PYJgt_qMDpv3vgSOs8f2nFM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP355921.RAW0f8-4luowGrelDuBQw4PYJgt_qMDpv3vgSOs8f2nFM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP355921.RAW0f8-4luowGrelDuBQw4PYJgt_qMDpv3vgSOs8f2nFM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP355921.RAW0f8-4luowGrelDuBQw4PYJgt_qMDpv3vgSOs8f2nFM130_provenance.
- NP355921.RAW0f8-4luowGrelDuBQw4PYJgt_qMDpv3vgSOs8f2nFM130_assertion description "[Myotonic dystrophy is an autosomally dominant inherited disease in which system-wide abnormalities are caused by a triplet repeat expansion within the 3' untranslated region of the myotonic dystrophy protein kinase (DMPK) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355921.RAW0f8-4luowGrelDuBQw4PYJgt_qMDpv3vgSOs8f2nFM130_provenance.
- NP355921.RAW0f8-4luowGrelDuBQw4PYJgt_qMDpv3vgSOs8f2nFM130_assertion evidence source_evidence_literature NP355921.RAW0f8-4luowGrelDuBQw4PYJgt_qMDpv3vgSOs8f2nFM130_provenance.
- NP355921.RAW0f8-4luowGrelDuBQw4PYJgt_qMDpv3vgSOs8f2nFM130_assertion SIO_000772 8288237 NP355921.RAW0f8-4luowGrelDuBQw4PYJgt_qMDpv3vgSOs8f2nFM130_provenance.
- NP355921.RAW0f8-4luowGrelDuBQw4PYJgt_qMDpv3vgSOs8f2nFM130_assertion wasDerivedFrom befree-20150227 NP355921.RAW0f8-4luowGrelDuBQw4PYJgt_qMDpv3vgSOs8f2nFM130_provenance.
- NP355921.RAW0f8-4luowGrelDuBQw4PYJgt_qMDpv3vgSOs8f2nFM130_assertion wasGeneratedBy ECO_0000203 NP355921.RAW0f8-4luowGrelDuBQw4PYJgt_qMDpv3vgSOs8f2nFM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP355921.RAW0f8-4luowGrelDuBQw4PYJgt_qMDpv3vgSOs8f2nFM130_provenance.