Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP260227.RAheXcIrucEfgBnrxs-cFD0qdmdsIcJ7fOgtCQnEcz_fE130_assertion> ?p ?o ?g. }
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- NP260227.RAheXcIrucEfgBnrxs-cFD0qdmdsIcJ7fOgtCQnEcz_fE130_assertion type Assertion NP260227.RAheXcIrucEfgBnrxs-cFD0qdmdsIcJ7fOgtCQnEcz_fE130_head.
- NP260227.RAheXcIrucEfgBnrxs-cFD0qdmdsIcJ7fOgtCQnEcz_fE130_assertion description "[The two males and the two obligate carrier females presented a mutation in the MECP2 gene, demonstrating that, in males, MECP2 can be responsible for severe mental retardation associated with neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP260227.RAheXcIrucEfgBnrxs-cFD0qdmdsIcJ7fOgtCQnEcz_fE130_provenance.
- NP260227.RAheXcIrucEfgBnrxs-cFD0qdmdsIcJ7fOgtCQnEcz_fE130_assertion evidence source_evidence_literature NP260227.RAheXcIrucEfgBnrxs-cFD0qdmdsIcJ7fOgtCQnEcz_fE130_provenance.
- NP260227.RAheXcIrucEfgBnrxs-cFD0qdmdsIcJ7fOgtCQnEcz_fE130_assertion SIO_000772 10986043 NP260227.RAheXcIrucEfgBnrxs-cFD0qdmdsIcJ7fOgtCQnEcz_fE130_provenance.
- NP260227.RAheXcIrucEfgBnrxs-cFD0qdmdsIcJ7fOgtCQnEcz_fE130_assertion wasDerivedFrom befree-20140225 NP260227.RAheXcIrucEfgBnrxs-cFD0qdmdsIcJ7fOgtCQnEcz_fE130_provenance.
- NP260227.RAheXcIrucEfgBnrxs-cFD0qdmdsIcJ7fOgtCQnEcz_fE130_assertion wasGeneratedBy ECO_0000203 NP260227.RAheXcIrucEfgBnrxs-cFD0qdmdsIcJ7fOgtCQnEcz_fE130_provenance.