Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1116218.RAVIWwreSmyC6HmVbGE2luextVl4edIdmKi-P19tFcVCU130_assertion> ?p ?o ?g. }
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- NP1116218.RAVIWwreSmyC6HmVbGE2luextVl4edIdmKi-P19tFcVCU130_assertion type Assertion NP1116218.RAVIWwreSmyC6HmVbGE2luextVl4edIdmKi-P19tFcVCU130_head.
- NP1116218.RAVIWwreSmyC6HmVbGE2luextVl4edIdmKi-P19tFcVCU130_assertion description "[Rett syndrome (RTT) is caused by mutations of MECP2, a methyl CpG binding protein thought to act as a global transcriptional repressor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1116218.RAVIWwreSmyC6HmVbGE2luextVl4edIdmKi-P19tFcVCU130_provenance.
- NP1116218.RAVIWwreSmyC6HmVbGE2luextVl4edIdmKi-P19tFcVCU130_assertion evidence source_evidence_literature NP1116218.RAVIWwreSmyC6HmVbGE2luextVl4edIdmKi-P19tFcVCU130_provenance.
- NP1116218.RAVIWwreSmyC6HmVbGE2luextVl4edIdmKi-P19tFcVCU130_assertion SIO_000772 24094325 NP1116218.RAVIWwreSmyC6HmVbGE2luextVl4edIdmKi-P19tFcVCU130_provenance.
- NP1116218.RAVIWwreSmyC6HmVbGE2luextVl4edIdmKi-P19tFcVCU130_assertion wasDerivedFrom befree-2016 NP1116218.RAVIWwreSmyC6HmVbGE2luextVl4edIdmKi-P19tFcVCU130_provenance.
- NP1116218.RAVIWwreSmyC6HmVbGE2luextVl4edIdmKi-P19tFcVCU130_assertion wasGeneratedBy ECO_0000203 NP1116218.RAVIWwreSmyC6HmVbGE2luextVl4edIdmKi-P19tFcVCU130_provenance.