Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP490377.RAdi61wxDeEuU4RJ4K8yMkQbNntKYhDwdn5vi0cCXezY8130_assertion> ?p ?o ?g. }
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- NP490377.RAdi61wxDeEuU4RJ4K8yMkQbNntKYhDwdn5vi0cCXezY8130_assertion type Assertion NP490377.RAdi61wxDeEuU4RJ4K8yMkQbNntKYhDwdn5vi0cCXezY8130_head.
- NP490377.RAdi61wxDeEuU4RJ4K8yMkQbNntKYhDwdn5vi0cCXezY8130_assertion wasGeneratedBy ECO_0000203 NP490377.RAdi61wxDeEuU4RJ4K8yMkQbNntKYhDwdn5vi0cCXezY8130_provenance.
- NP490377.RAdi61wxDeEuU4RJ4K8yMkQbNntKYhDwdn5vi0cCXezY8130_assertion wasDerivedFrom befree-20140225 NP490377.RAdi61wxDeEuU4RJ4K8yMkQbNntKYhDwdn5vi0cCXezY8130_provenance.
- NP490377.RAdi61wxDeEuU4RJ4K8yMkQbNntKYhDwdn5vi0cCXezY8130_assertion SIO_000772 18499664 NP490377.RAdi61wxDeEuU4RJ4K8yMkQbNntKYhDwdn5vi0cCXezY8130_provenance.
- NP490377.RAdi61wxDeEuU4RJ4K8yMkQbNntKYhDwdn5vi0cCXezY8130_assertion evidence source_evidence_literature NP490377.RAdi61wxDeEuU4RJ4K8yMkQbNntKYhDwdn5vi0cCXezY8130_provenance.
- NP490377.RAdi61wxDeEuU4RJ4K8yMkQbNntKYhDwdn5vi0cCXezY8130_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." NP490377.RAdi61wxDeEuU4RJ4K8yMkQbNntKYhDwdn5vi0cCXezY8130_provenance.