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- NP355921.RAW0f8-4luowGrelDuBQw4PYJgt_qMDpv3vgSOs8f2nFM130_assertion type Assertion NP355921.RAW0f8-4luowGrelDuBQw4PYJgt_qMDpv3vgSOs8f2nFM130_head.
- 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.