Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP621019.RALz7cBhwMs-WbKd1QhJxfBTt2iLyfw73YoeGl90sEidY130_assertion> ?p ?o ?g. }
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- NP621019.RALz7cBhwMs-WbKd1QhJxfBTt2iLyfw73YoeGl90sEidY130_assertion type Assertion NP621019.RALz7cBhwMs-WbKd1QhJxfBTt2iLyfw73YoeGl90sEidY130_head.
- NP621019.RALz7cBhwMs-WbKd1QhJxfBTt2iLyfw73YoeGl90sEidY130_assertion description "[We suggest that these features, in particular severe developmental delay and epilepsy, may form part of the characteristic phenotype resulting from deletion of both FMR1 and FMR2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621019.RALz7cBhwMs-WbKd1QhJxfBTt2iLyfw73YoeGl90sEidY130_provenance.
- NP621019.RALz7cBhwMs-WbKd1QhJxfBTt2iLyfw73YoeGl90sEidY130_assertion evidence source_evidence_literature NP621019.RALz7cBhwMs-WbKd1QhJxfBTt2iLyfw73YoeGl90sEidY130_provenance.
- NP621019.RALz7cBhwMs-WbKd1QhJxfBTt2iLyfw73YoeGl90sEidY130_assertion SIO_000772 10424820 NP621019.RALz7cBhwMs-WbKd1QhJxfBTt2iLyfw73YoeGl90sEidY130_provenance.
- NP621019.RALz7cBhwMs-WbKd1QhJxfBTt2iLyfw73YoeGl90sEidY130_assertion wasDerivedFrom befree-20140225 NP621019.RALz7cBhwMs-WbKd1QhJxfBTt2iLyfw73YoeGl90sEidY130_provenance.
- NP621019.RALz7cBhwMs-WbKd1QhJxfBTt2iLyfw73YoeGl90sEidY130_assertion wasGeneratedBy ECO_0000203 NP621019.RALz7cBhwMs-WbKd1QhJxfBTt2iLyfw73YoeGl90sEidY130_provenance.