Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_assertion> ?p ?o ?g. }
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- NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_assertion type Assertion NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_head.
- NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_assertion description "[Rett syndrome, a neurodevelopmental disorder caused by mutations in the X-linked gene encoding methyl-CpG-binding protein 2 (MeCP2), is a leading cause of mental retardation with autistic features in females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_provenance.
- NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_assertion evidence source_evidence_literature NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_provenance.
- NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_assertion SIO_000772 16647848 NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_provenance.
- NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_assertion wasDerivedFrom befree-2016 NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_provenance.
- NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_assertion wasGeneratedBy ECO_0000203 NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_provenance.