Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP780157.RAEP7t-_Jse2dYJOWau9MVpZcK0PcEv9AOvf_z-AKHABA130_assertion> ?p ?o ?g. }
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- NP780157.RAEP7t-_Jse2dYJOWau9MVpZcK0PcEv9AOvf_z-AKHABA130_assertion type Assertion NP780157.RAEP7t-_Jse2dYJOWau9MVpZcK0PcEv9AOvf_z-AKHABA130_head.
- NP780157.RAEP7t-_Jse2dYJOWau9MVpZcK0PcEv9AOvf_z-AKHABA130_assertion wasGeneratedBy ECO_0000203 NP780157.RAEP7t-_Jse2dYJOWau9MVpZcK0PcEv9AOvf_z-AKHABA130_provenance.
- NP780157.RAEP7t-_Jse2dYJOWau9MVpZcK0PcEv9AOvf_z-AKHABA130_assertion wasDerivedFrom befree-20140225 NP780157.RAEP7t-_Jse2dYJOWau9MVpZcK0PcEv9AOvf_z-AKHABA130_provenance.
- NP780157.RAEP7t-_Jse2dYJOWau9MVpZcK0PcEv9AOvf_z-AKHABA130_assertion SIO_000772 9748047 NP780157.RAEP7t-_Jse2dYJOWau9MVpZcK0PcEv9AOvf_z-AKHABA130_provenance.
- NP780157.RAEP7t-_Jse2dYJOWau9MVpZcK0PcEv9AOvf_z-AKHABA130_assertion evidence source_evidence_literature NP780157.RAEP7t-_Jse2dYJOWau9MVpZcK0PcEv9AOvf_z-AKHABA130_provenance.
- NP780157.RAEP7t-_Jse2dYJOWau9MVpZcK0PcEv9AOvf_z-AKHABA130_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." NP780157.RAEP7t-_Jse2dYJOWau9MVpZcK0PcEv9AOvf_z-AKHABA130_provenance.