Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP279146.RAVXA4cOIrRRjbNfNoQC92nGsSIC3kC9o-KMWl91DLG8w130_assertion> ?p ?o ?g. }
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- NP279146.RAVXA4cOIrRRjbNfNoQC92nGsSIC3kC9o-KMWl91DLG8w130_assertion type Assertion NP279146.RAVXA4cOIrRRjbNfNoQC92nGsSIC3kC9o-KMWl91DLG8w130_head.
- NP279146.RAVXA4cOIrRRjbNfNoQC92nGsSIC3kC9o-KMWl91DLG8w130_assertion description "[Although ubiquitously expressed, DNM2 was found mutated in two genetic disorders affecting different tissues: autosomal dominant centronuclear myopathy (ADCNM; skeletal muscle) and peripheral Charcot-Marie-Tooth neuropathy (peripheral nerve).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279146.RAVXA4cOIrRRjbNfNoQC92nGsSIC3kC9o-KMWl91DLG8w130_provenance.
- NP279146.RAVXA4cOIrRRjbNfNoQC92nGsSIC3kC9o-KMWl91DLG8w130_assertion evidence source_evidence_literature NP279146.RAVXA4cOIrRRjbNfNoQC92nGsSIC3kC9o-KMWl91DLG8w130_provenance.
- NP279146.RAVXA4cOIrRRjbNfNoQC92nGsSIC3kC9o-KMWl91DLG8w130_assertion SIO_000772 21514436 NP279146.RAVXA4cOIrRRjbNfNoQC92nGsSIC3kC9o-KMWl91DLG8w130_provenance.
- NP279146.RAVXA4cOIrRRjbNfNoQC92nGsSIC3kC9o-KMWl91DLG8w130_assertion wasDerivedFrom befree-20140225 NP279146.RAVXA4cOIrRRjbNfNoQC92nGsSIC3kC9o-KMWl91DLG8w130_provenance.
- NP279146.RAVXA4cOIrRRjbNfNoQC92nGsSIC3kC9o-KMWl91DLG8w130_assertion wasGeneratedBy ECO_0000203 NP279146.RAVXA4cOIrRRjbNfNoQC92nGsSIC3kC9o-KMWl91DLG8w130_provenance.