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- NP595027.RAkS22UK3jluryY19u1vsLLNPxeJ4vMSQmrXP3TODRdtQ130_assertion type Assertion NP595027.RAkS22UK3jluryY19u1vsLLNPxeJ4vMSQmrXP3TODRdtQ130_head.
- NP595027.RAkS22UK3jluryY19u1vsLLNPxeJ4vMSQmrXP3TODRdtQ130_assertion description "[Mutations in the X-chromosomal gene (L1CAM) for cell adhesion molecule L1 are associated with a heterogeneous group of conditions that include agenesis of the corpus callosum, hydrocephalus, spastic paraplegia, adducted thumbs and mental retardation (L1-spectrum disease, CRASH or MASA syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595027.RAkS22UK3jluryY19u1vsLLNPxeJ4vMSQmrXP3TODRdtQ130_provenance.
- NP595027.RAkS22UK3jluryY19u1vsLLNPxeJ4vMSQmrXP3TODRdtQ130_assertion evidence source_evidence_literature NP595027.RAkS22UK3jluryY19u1vsLLNPxeJ4vMSQmrXP3TODRdtQ130_provenance.
- NP595027.RAkS22UK3jluryY19u1vsLLNPxeJ4vMSQmrXP3TODRdtQ130_assertion SIO_000772 17294222 NP595027.RAkS22UK3jluryY19u1vsLLNPxeJ4vMSQmrXP3TODRdtQ130_provenance.
- NP595027.RAkS22UK3jluryY19u1vsLLNPxeJ4vMSQmrXP3TODRdtQ130_assertion wasDerivedFrom befree-20140225 NP595027.RAkS22UK3jluryY19u1vsLLNPxeJ4vMSQmrXP3TODRdtQ130_provenance.
- NP595027.RAkS22UK3jluryY19u1vsLLNPxeJ4vMSQmrXP3TODRdtQ130_assertion wasGeneratedBy ECO_0000203 NP595027.RAkS22UK3jluryY19u1vsLLNPxeJ4vMSQmrXP3TODRdtQ130_provenance.