Matches in Nanopublications for { <http://krauthammerlab.med.yale.edu/nanopub/GeneRIF272089.RAQJk_j9c_b6Is71uHGbwhUwswlhchFciz3429f-5Cg0k#assertion> ?p ?o ?g. }
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- assertion type UnderspecifiedAssertion assertion.
- assertion hadPrimarySource 22123427 provenance.
- assertion wasDerivedFrom generifs_basic.gz provenance.
- assertion about 9606 assertion.
- assertion about 4204 assertion.
- assertion asSentence Sequencing+of+exons+1+to+4+of+MECP2+is+recommended+for+patients+with+a+Rett+syndrome+phenotype%2C+unexplained+neonatal+encephalopathy%2C+an+Angelman+syndrome+phenotype%2C+nonspecific+mental+retardation%2C+or+autism+%28females%29. assertion.