Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP827261.RA4VmdMrhOXKlNTJtuY_pDz1R0z90n_RRbGev6LzQC_sc130_assertion> ?p ?o ?g. }
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- NP827261.RA4VmdMrhOXKlNTJtuY_pDz1R0z90n_RRbGev6LzQC_sc130_assertion type Assertion NP827261.RA4VmdMrhOXKlNTJtuY_pDz1R0z90n_RRbGev6LzQC_sc130_head.
- NP827261.RA4VmdMrhOXKlNTJtuY_pDz1R0z90n_RRbGev6LzQC_sc130_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." NP827261.RA4VmdMrhOXKlNTJtuY_pDz1R0z90n_RRbGev6LzQC_sc130_provenance.
- NP827261.RA4VmdMrhOXKlNTJtuY_pDz1R0z90n_RRbGev6LzQC_sc130_assertion evidence source_evidence_literature NP827261.RA4VmdMrhOXKlNTJtuY_pDz1R0z90n_RRbGev6LzQC_sc130_provenance.
- NP827261.RA4VmdMrhOXKlNTJtuY_pDz1R0z90n_RRbGev6LzQC_sc130_assertion SIO_000772 12921235 NP827261.RA4VmdMrhOXKlNTJtuY_pDz1R0z90n_RRbGev6LzQC_sc130_provenance.
- NP827261.RA4VmdMrhOXKlNTJtuY_pDz1R0z90n_RRbGev6LzQC_sc130_assertion wasDerivedFrom befree-20150227 NP827261.RA4VmdMrhOXKlNTJtuY_pDz1R0z90n_RRbGev6LzQC_sc130_provenance.
- NP827261.RA4VmdMrhOXKlNTJtuY_pDz1R0z90n_RRbGev6LzQC_sc130_assertion wasGeneratedBy ECO_0000203 NP827261.RA4VmdMrhOXKlNTJtuY_pDz1R0z90n_RRbGev6LzQC_sc130_provenance.