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- NP169368.RAPautxdOVQgBNH--GmYvKBqEzwRgV81eNrG8rwpN81gc130_assertion type Assertion NP169368.RAPautxdOVQgBNH--GmYvKBqEzwRgV81eNrG8rwpN81gc130_head.
- NP169368.RAPautxdOVQgBNH--GmYvKBqEzwRgV81eNrG8rwpN81gc130_assertion description "[Myotonic dystrophy types 1 (DM1) and 2 (DM2/proximal myotonic myopathy PROMM) are dominantly inherited disorders with unusual multisystemic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP169368.RAPautxdOVQgBNH--GmYvKBqEzwRgV81eNrG8rwpN81gc130_provenance.
- NP169368.RAPautxdOVQgBNH--GmYvKBqEzwRgV81eNrG8rwpN81gc130_assertion evidence source_evidence_literature NP169368.RAPautxdOVQgBNH--GmYvKBqEzwRgV81eNrG8rwpN81gc130_provenance.
- NP169368.RAPautxdOVQgBNH--GmYvKBqEzwRgV81eNrG8rwpN81gc130_assertion SIO_000772 12601109 NP169368.RAPautxdOVQgBNH--GmYvKBqEzwRgV81eNrG8rwpN81gc130_provenance.
- NP169368.RAPautxdOVQgBNH--GmYvKBqEzwRgV81eNrG8rwpN81gc130_assertion wasDerivedFrom befree-20140225 NP169368.RAPautxdOVQgBNH--GmYvKBqEzwRgV81eNrG8rwpN81gc130_provenance.
- NP169368.RAPautxdOVQgBNH--GmYvKBqEzwRgV81eNrG8rwpN81gc130_assertion wasGeneratedBy ECO_0000203 NP169368.RAPautxdOVQgBNH--GmYvKBqEzwRgV81eNrG8rwpN81gc130_provenance.