Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP384692.RAcngyXd3bSfa3-XROsZSg1QRlSMiZsURXE3_PJbn0woY130_assertion> ?p ?o ?g. }
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- NP384692.RAcngyXd3bSfa3-XROsZSg1QRlSMiZsURXE3_PJbn0woY130_assertion type Assertion NP384692.RAcngyXd3bSfa3-XROsZSg1QRlSMiZsURXE3_PJbn0woY130_head.
- NP384692.RAcngyXd3bSfa3-XROsZSg1QRlSMiZsURXE3_PJbn0woY130_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." NP384692.RAcngyXd3bSfa3-XROsZSg1QRlSMiZsURXE3_PJbn0woY130_provenance.
- NP384692.RAcngyXd3bSfa3-XROsZSg1QRlSMiZsURXE3_PJbn0woY130_assertion evidence source_evidence_literature NP384692.RAcngyXd3bSfa3-XROsZSg1QRlSMiZsURXE3_PJbn0woY130_provenance.
- NP384692.RAcngyXd3bSfa3-XROsZSg1QRlSMiZsURXE3_PJbn0woY130_assertion SIO_000772 12601109 NP384692.RAcngyXd3bSfa3-XROsZSg1QRlSMiZsURXE3_PJbn0woY130_provenance.
- NP384692.RAcngyXd3bSfa3-XROsZSg1QRlSMiZsURXE3_PJbn0woY130_assertion wasDerivedFrom befree-2016 NP384692.RAcngyXd3bSfa3-XROsZSg1QRlSMiZsURXE3_PJbn0woY130_provenance.
- NP384692.RAcngyXd3bSfa3-XROsZSg1QRlSMiZsURXE3_PJbn0woY130_assertion wasGeneratedBy ECO_0000203 NP384692.RAcngyXd3bSfa3-XROsZSg1QRlSMiZsURXE3_PJbn0woY130_provenance.