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- NP496225.RAM3xFq2sm0GKET-bSG-yFHQdw0qNHHAiuiu7a55Q0Cts130_assertion type Assertion NP496225.RAM3xFq2sm0GKET-bSG-yFHQdw0qNHHAiuiu7a55Q0Cts130_head.
- NP496225.RAM3xFq2sm0GKET-bSG-yFHQdw0qNHHAiuiu7a55Q0Cts130_assertion description "[Novel point mutation in the NKX2-5 gene in a Moroccan family with atrioventricular conduction disturbance and an atrial septal defect in the oval fossa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496225.RAM3xFq2sm0GKET-bSG-yFHQdw0qNHHAiuiu7a55Q0Cts130_provenance.
- NP496225.RAM3xFq2sm0GKET-bSG-yFHQdw0qNHHAiuiu7a55Q0Cts130_assertion evidence source_evidence_literature NP496225.RAM3xFq2sm0GKET-bSG-yFHQdw0qNHHAiuiu7a55Q0Cts130_provenance.
- NP496225.RAM3xFq2sm0GKET-bSG-yFHQdw0qNHHAiuiu7a55Q0Cts130_assertion SIO_000772 17184575 NP496225.RAM3xFq2sm0GKET-bSG-yFHQdw0qNHHAiuiu7a55Q0Cts130_provenance.
- NP496225.RAM3xFq2sm0GKET-bSG-yFHQdw0qNHHAiuiu7a55Q0Cts130_assertion wasDerivedFrom befree-20140225 NP496225.RAM3xFq2sm0GKET-bSG-yFHQdw0qNHHAiuiu7a55Q0Cts130_provenance.
- NP496225.RAM3xFq2sm0GKET-bSG-yFHQdw0qNHHAiuiu7a55Q0Cts130_assertion wasGeneratedBy ECO_0000203 NP496225.RAM3xFq2sm0GKET-bSG-yFHQdw0qNHHAiuiu7a55Q0Cts130_provenance.