Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP867761.RA74gTG01wxstIMhMcIS1KnUQH_NzGUSpVUpJs0Pu9H6w130_assertion> ?p ?o ?g. }
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- NP867761.RA74gTG01wxstIMhMcIS1KnUQH_NzGUSpVUpJs0Pu9H6w130_assertion type Assertion NP867761.RA74gTG01wxstIMhMcIS1KnUQH_NzGUSpVUpJs0Pu9H6w130_head.
- NP867761.RA74gTG01wxstIMhMcIS1KnUQH_NzGUSpVUpJs0Pu9H6w130_assertion description "[Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867761.RA74gTG01wxstIMhMcIS1KnUQH_NzGUSpVUpJs0Pu9H6w130_provenance.
- NP867761.RA74gTG01wxstIMhMcIS1KnUQH_NzGUSpVUpJs0Pu9H6w130_assertion evidence source_evidence_literature NP867761.RA74gTG01wxstIMhMcIS1KnUQH_NzGUSpVUpJs0Pu9H6w130_provenance.
- NP867761.RA74gTG01wxstIMhMcIS1KnUQH_NzGUSpVUpJs0Pu9H6w130_assertion SIO_000772 21267004 NP867761.RA74gTG01wxstIMhMcIS1KnUQH_NzGUSpVUpJs0Pu9H6w130_provenance.
- NP867761.RA74gTG01wxstIMhMcIS1KnUQH_NzGUSpVUpJs0Pu9H6w130_assertion wasDerivedFrom befree-2016 NP867761.RA74gTG01wxstIMhMcIS1KnUQH_NzGUSpVUpJs0Pu9H6w130_provenance.
- NP867761.RA74gTG01wxstIMhMcIS1KnUQH_NzGUSpVUpJs0Pu9H6w130_assertion wasGeneratedBy ECO_0000203 NP867761.RA74gTG01wxstIMhMcIS1KnUQH_NzGUSpVUpJs0Pu9H6w130_provenance.