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- NP870183.RAfE1KCYjhBOyxNIpIVkCIDuBIGATth11g63eWBKgCWwA130_assertion type Assertion NP870183.RAfE1KCYjhBOyxNIpIVkCIDuBIGATth11g63eWBKgCWwA130_head.
- NP870183.RAfE1KCYjhBOyxNIpIVkCIDuBIGATth11g63eWBKgCWwA130_assertion description "[The index patient was homozygous for a 3889C>T nonsense mutation in the VPS13A gene and presented with a typical ChAc phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870183.RAfE1KCYjhBOyxNIpIVkCIDuBIGATth11g63eWBKgCWwA130_provenance.
- NP870183.RAfE1KCYjhBOyxNIpIVkCIDuBIGATth11g63eWBKgCWwA130_assertion evidence source_evidence_literature NP870183.RAfE1KCYjhBOyxNIpIVkCIDuBIGATth11g63eWBKgCWwA130_provenance.
- NP870183.RAfE1KCYjhBOyxNIpIVkCIDuBIGATth11g63eWBKgCWwA130_assertion SIO_000772 17673232 NP870183.RAfE1KCYjhBOyxNIpIVkCIDuBIGATth11g63eWBKgCWwA130_provenance.
- NP870183.RAfE1KCYjhBOyxNIpIVkCIDuBIGATth11g63eWBKgCWwA130_assertion wasDerivedFrom befree-20150227 NP870183.RAfE1KCYjhBOyxNIpIVkCIDuBIGATth11g63eWBKgCWwA130_provenance.
- NP870183.RAfE1KCYjhBOyxNIpIVkCIDuBIGATth11g63eWBKgCWwA130_assertion wasGeneratedBy ECO_0000203 NP870183.RAfE1KCYjhBOyxNIpIVkCIDuBIGATth11g63eWBKgCWwA130_provenance.