Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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." provenance.
- 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." provenance.
- 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.
- NP896548.RAA_gjDheqzdzeLhNreYf8ErEHMrI0e6z_RyV_qd6ZIOc130_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." NP896548.RAA_gjDheqzdzeLhNreYf8ErEHMrI0e6z_RyV_qd6ZIOc130_provenance.
- NP1116219.RAGg5caEQ9GKCVdGN6bL8OdXDLOgp03JLtBssx0cBGRjQ130_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." NP1116219.RAGg5caEQ9GKCVdGN6bL8OdXDLOgp03JLtBssx0cBGRjQ130_provenance.