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- NP592200.RAWvgi48_F5Poy1HlGP293TWLzydnMFRy8nhref-sczfs130_assertion type Assertion NP592200.RAWvgi48_F5Poy1HlGP293TWLzydnMFRy8nhref-sczfs130_head.
- NP592200.RAWvgi48_F5Poy1HlGP293TWLzydnMFRy8nhref-sczfs130_assertion wasGeneratedBy ECO_0000203 NP592200.RAWvgi48_F5Poy1HlGP293TWLzydnMFRy8nhref-sczfs130_provenance.
- NP592200.RAWvgi48_F5Poy1HlGP293TWLzydnMFRy8nhref-sczfs130_assertion wasDerivedFrom befree-2016 NP592200.RAWvgi48_F5Poy1HlGP293TWLzydnMFRy8nhref-sczfs130_provenance.
- NP592200.RAWvgi48_F5Poy1HlGP293TWLzydnMFRy8nhref-sczfs130_assertion SIO_000772 17276711 NP592200.RAWvgi48_F5Poy1HlGP293TWLzydnMFRy8nhref-sczfs130_provenance.
- NP592200.RAWvgi48_F5Poy1HlGP293TWLzydnMFRy8nhref-sczfs130_assertion evidence source_evidence_literature NP592200.RAWvgi48_F5Poy1HlGP293TWLzydnMFRy8nhref-sczfs130_provenance.
- NP592200.RAWvgi48_F5Poy1HlGP293TWLzydnMFRy8nhref-sczfs130_assertion description "[Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592200.RAWvgi48_F5Poy1HlGP293TWLzydnMFRy8nhref-sczfs130_provenance.