Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP672822.RAks7coYGhiEsE4F0AGJkHaw8E2xusDl2cqZAt8tGNg5g130_assertion> ?p ?o ?g. }
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- NP672822.RAks7coYGhiEsE4F0AGJkHaw8E2xusDl2cqZAt8tGNg5g130_assertion type Assertion NP672822.RAks7coYGhiEsE4F0AGJkHaw8E2xusDl2cqZAt8tGNg5g130_head.
- NP672822.RAks7coYGhiEsE4F0AGJkHaw8E2xusDl2cqZAt8tGNg5g130_assertion wasGeneratedBy ECO_0000203 NP672822.RAks7coYGhiEsE4F0AGJkHaw8E2xusDl2cqZAt8tGNg5g130_provenance.
- NP672822.RAks7coYGhiEsE4F0AGJkHaw8E2xusDl2cqZAt8tGNg5g130_assertion wasDerivedFrom befree-2016 NP672822.RAks7coYGhiEsE4F0AGJkHaw8E2xusDl2cqZAt8tGNg5g130_provenance.
- NP672822.RAks7coYGhiEsE4F0AGJkHaw8E2xusDl2cqZAt8tGNg5g130_assertion SIO_000772 18499664 NP672822.RAks7coYGhiEsE4F0AGJkHaw8E2xusDl2cqZAt8tGNg5g130_provenance.
- NP672822.RAks7coYGhiEsE4F0AGJkHaw8E2xusDl2cqZAt8tGNg5g130_assertion evidence source_evidence_literature NP672822.RAks7coYGhiEsE4F0AGJkHaw8E2xusDl2cqZAt8tGNg5g130_provenance.
- NP672822.RAks7coYGhiEsE4F0AGJkHaw8E2xusDl2cqZAt8tGNg5g130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672822.RAks7coYGhiEsE4F0AGJkHaw8E2xusDl2cqZAt8tGNg5g130_provenance.