Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP509216.RADgIfsHrqywErP85S7M1Z6qkr6mtIY0p4am8C5YzBEmw130_assertion> ?p ?o ?g. }
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- NP509216.RADgIfsHrqywErP85S7M1Z6qkr6mtIY0p4am8C5YzBEmw130_assertion type Assertion NP509216.RADgIfsHrqywErP85S7M1Z6qkr6mtIY0p4am8C5YzBEmw130_head.
- NP509216.RADgIfsHrqywErP85S7M1Z6qkr6mtIY0p4am8C5YzBEmw130_assertion description "[These diseases include Emery-Dreifuss muscular dystrophy, limb girdle muscular dystrophy, dilated cardiomyopathy (DCM) with conduction system disease, familial partial lipodystrophy (FPLD), autosomal recessive axonal neuropathy (Charcot-Marie-Tooth disorder type 2, CMT2), mandibuloacral dysplasia (MAD), Hutchison Gilford Progeria syndrome (HGS), Greenberg Skeletal Dysplasia, and Pelger-Huet anomaly (PHA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP509216.RADgIfsHrqywErP85S7M1Z6qkr6mtIY0p4am8C5YzBEmw130_provenance.
- NP509216.RADgIfsHrqywErP85S7M1Z6qkr6mtIY0p4am8C5YzBEmw130_assertion evidence source_evidence_literature NP509216.RADgIfsHrqywErP85S7M1Z6qkr6mtIY0p4am8C5YzBEmw130_provenance.
- NP509216.RADgIfsHrqywErP85S7M1Z6qkr6mtIY0p4am8C5YzBEmw130_assertion SIO_000772 12921235 NP509216.RADgIfsHrqywErP85S7M1Z6qkr6mtIY0p4am8C5YzBEmw130_provenance.
- NP509216.RADgIfsHrqywErP85S7M1Z6qkr6mtIY0p4am8C5YzBEmw130_assertion wasDerivedFrom befree-20140225 NP509216.RADgIfsHrqywErP85S7M1Z6qkr6mtIY0p4am8C5YzBEmw130_provenance.
- NP509216.RADgIfsHrqywErP85S7M1Z6qkr6mtIY0p4am8C5YzBEmw130_assertion wasGeneratedBy ECO_0000203 NP509216.RADgIfsHrqywErP85S7M1Z6qkr6mtIY0p4am8C5YzBEmw130_provenance.