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- NP462905.RA1OU8SJpM3d0Rsbgdat1oxmnOwedZA6Vs3G4CSxAFuK8130_assertion type Assertion NP462905.RA1OU8SJpM3d0Rsbgdat1oxmnOwedZA6Vs3G4CSxAFuK8130_head.
- NP462905.RA1OU8SJpM3d0Rsbgdat1oxmnOwedZA6Vs3G4CSxAFuK8130_assertion wasGeneratedBy ECO_0000203 NP462905.RA1OU8SJpM3d0Rsbgdat1oxmnOwedZA6Vs3G4CSxAFuK8130_provenance.
- NP462905.RA1OU8SJpM3d0Rsbgdat1oxmnOwedZA6Vs3G4CSxAFuK8130_assertion wasDerivedFrom befree-20140225 NP462905.RA1OU8SJpM3d0Rsbgdat1oxmnOwedZA6Vs3G4CSxAFuK8130_provenance.
- NP462905.RA1OU8SJpM3d0Rsbgdat1oxmnOwedZA6Vs3G4CSxAFuK8130_assertion SIO_000772 9748047 NP462905.RA1OU8SJpM3d0Rsbgdat1oxmnOwedZA6Vs3G4CSxAFuK8130_provenance.
- NP462905.RA1OU8SJpM3d0Rsbgdat1oxmnOwedZA6Vs3G4CSxAFuK8130_assertion evidence source_evidence_literature NP462905.RA1OU8SJpM3d0Rsbgdat1oxmnOwedZA6Vs3G4CSxAFuK8130_provenance.
- NP462905.RA1OU8SJpM3d0Rsbgdat1oxmnOwedZA6Vs3G4CSxAFuK8130_assertion description "[A Chinese male infant with arthrogryposis multiplex congenita (AMC), ventricular and atrial septal defects, and Werdnig-Hoffmann disease (WHD) had deletions of the telomeric copy of the survival motor neuron (SMN(T)) and neuronal apoptosis inhibitory protein genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP462905.RA1OU8SJpM3d0Rsbgdat1oxmnOwedZA6Vs3G4CSxAFuK8130_provenance.