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- NP766041.RADWR8s1QgajpiWcAIxqc3URcpKgE8uKVBYumGY_-JSNo130_assertion type Assertion NP766041.RADWR8s1QgajpiWcAIxqc3URcpKgE8uKVBYumGY_-JSNo130_head.
- NP766041.RADWR8s1QgajpiWcAIxqc3URcpKgE8uKVBYumGY_-JSNo130_assertion wasGeneratedBy ECO_0000203 NP766041.RADWR8s1QgajpiWcAIxqc3URcpKgE8uKVBYumGY_-JSNo130_provenance.
- NP766041.RADWR8s1QgajpiWcAIxqc3URcpKgE8uKVBYumGY_-JSNo130_assertion wasDerivedFrom befree-20140225 NP766041.RADWR8s1QgajpiWcAIxqc3URcpKgE8uKVBYumGY_-JSNo130_provenance.
- NP766041.RADWR8s1QgajpiWcAIxqc3URcpKgE8uKVBYumGY_-JSNo130_assertion SIO_000772 18405873 NP766041.RADWR8s1QgajpiWcAIxqc3URcpKgE8uKVBYumGY_-JSNo130_provenance.
- NP766041.RADWR8s1QgajpiWcAIxqc3URcpKgE8uKVBYumGY_-JSNo130_assertion evidence source_evidence_literature NP766041.RADWR8s1QgajpiWcAIxqc3URcpKgE8uKVBYumGY_-JSNo130_provenance.
- NP766041.RADWR8s1QgajpiWcAIxqc3URcpKgE8uKVBYumGY_-JSNo130_assertion description "[We have identified and characterized two unrelated patients with prenatal onset of microcephaly, intrauterine growth retardation, feeding problems, developmental delay, and febrile seizures/epilepsy who both carry a de novo balanced translocation that truncates the DYRK1A gene at chromosome 21q22.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766041.RADWR8s1QgajpiWcAIxqc3URcpKgE8uKVBYumGY_-JSNo130_provenance.