Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP124202.RAI0Ra7_Gh9k2snn2ciygcuy7ppbPe9RRkYsp45SMlSyE130_assertion> ?p ?o ?g. }
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- NP124202.RAI0Ra7_Gh9k2snn2ciygcuy7ppbPe9RRkYsp45SMlSyE130_assertion type Assertion NP124202.RAI0Ra7_Gh9k2snn2ciygcuy7ppbPe9RRkYsp45SMlSyE130_head.
- NP124202.RAI0Ra7_Gh9k2snn2ciygcuy7ppbPe9RRkYsp45SMlSyE130_assertion description "[Considering genotype-phenotype correlation, we suggest screening of the most common mutation, the c.428 _ 451 dup mutation by PCR, in patients with infantile spasm syndrome, Partington syndrome and non-syndromic X-linked mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP124202.RAI0Ra7_Gh9k2snn2ciygcuy7ppbPe9RRkYsp45SMlSyE130_provenance.
- NP124202.RAI0Ra7_Gh9k2snn2ciygcuy7ppbPe9RRkYsp45SMlSyE130_assertion evidence source_evidence_literature NP124202.RAI0Ra7_Gh9k2snn2ciygcuy7ppbPe9RRkYsp45SMlSyE130_provenance.
- NP124202.RAI0Ra7_Gh9k2snn2ciygcuy7ppbPe9RRkYsp45SMlSyE130_assertion SIO_000772 17613295 NP124202.RAI0Ra7_Gh9k2snn2ciygcuy7ppbPe9RRkYsp45SMlSyE130_provenance.
- NP124202.RAI0Ra7_Gh9k2snn2ciygcuy7ppbPe9RRkYsp45SMlSyE130_assertion wasDerivedFrom lhgdn-20090331 NP124202.RAI0Ra7_Gh9k2snn2ciygcuy7ppbPe9RRkYsp45SMlSyE130_provenance.
- NP124202.RAI0Ra7_Gh9k2snn2ciygcuy7ppbPe9RRkYsp45SMlSyE130_assertion wasGeneratedBy ECO_0000203 NP124202.RAI0Ra7_Gh9k2snn2ciygcuy7ppbPe9RRkYsp45SMlSyE130_provenance.