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- NP434576.RACd5osNk_cijd2hot2p3vjw4K9O4ZX8E16jOfKCnzf-M130_assertion type Assertion NP434576.RACd5osNk_cijd2hot2p3vjw4K9O4ZX8E16jOfKCnzf-M130_head.
- NP434576.RACd5osNk_cijd2hot2p3vjw4K9O4ZX8E16jOfKCnzf-M130_assertion description "[ZFHX1B mutations cause a complex developmental phenotype characterized by severe mental retardation (MR) and multiple congenital defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434576.RACd5osNk_cijd2hot2p3vjw4K9O4ZX8E16jOfKCnzf-M130_provenance.
- NP434576.RACd5osNk_cijd2hot2p3vjw4K9O4ZX8E16jOfKCnzf-M130_assertion evidence source_evidence_literature NP434576.RACd5osNk_cijd2hot2p3vjw4K9O4ZX8E16jOfKCnzf-M130_provenance.
- NP434576.RACd5osNk_cijd2hot2p3vjw4K9O4ZX8E16jOfKCnzf-M130_assertion SIO_000772 15006694 NP434576.RACd5osNk_cijd2hot2p3vjw4K9O4ZX8E16jOfKCnzf-M130_provenance.
- NP434576.RACd5osNk_cijd2hot2p3vjw4K9O4ZX8E16jOfKCnzf-M130_assertion wasDerivedFrom befree-2016 NP434576.RACd5osNk_cijd2hot2p3vjw4K9O4ZX8E16jOfKCnzf-M130_provenance.
- NP434576.RACd5osNk_cijd2hot2p3vjw4K9O4ZX8E16jOfKCnzf-M130_assertion wasGeneratedBy ECO_0000203 NP434576.RACd5osNk_cijd2hot2p3vjw4K9O4ZX8E16jOfKCnzf-M130_provenance.