Matches in Nanopublications for { ?s ?p "[MECP2 mutations cause the X-linked neurodevelopmental disorder Rett Syndrome (RTT) by consistently altering the protein encoded by the MECP2e1 alternative transcript.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[MECP2 mutations cause the X-linked neurodevelopmental disorder Rett Syndrome (RTT) by consistently altering the protein encoded by the MECP2e1 alternative transcript.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[MECP2 mutations cause the X-linked neurodevelopmental disorder Rett Syndrome (RTT) by consistently altering the protein encoded by the MECP2e1 alternative transcript.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1260358.RAdKQWQRR_UcmCQvjdYpgx4jwtiLqEHR5b6JD8DCN0Fsk130_assertion description "[MECP2 mutations cause the X-linked neurodevelopmental disorder Rett Syndrome (RTT) by consistently altering the protein encoded by the MECP2e1 alternative transcript.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260358.RAdKQWQRR_UcmCQvjdYpgx4jwtiLqEHR5b6JD8DCN0Fsk130_provenance.
- NP1260357.RAt9NxHJM-_FEM55ovNQ-HNkTOxYYDwRTyD3-dMOygpfs130_assertion description "[MECP2 mutations cause the X-linked neurodevelopmental disorder Rett Syndrome (RTT) by consistently altering the protein encoded by the MECP2e1 alternative transcript.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260357.RAt9NxHJM-_FEM55ovNQ-HNkTOxYYDwRTyD3-dMOygpfs130_provenance.