Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP210833.RA0sgjN1LIwyj_7qzNxQq5zmvjRrc6xjzSvkSrQ7dtmXI130_assertion> ?p ?o ?g. }
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- NP210833.RA0sgjN1LIwyj_7qzNxQq5zmvjRrc6xjzSvkSrQ7dtmXI130_assertion type Assertion NP210833.RA0sgjN1LIwyj_7qzNxQq5zmvjRrc6xjzSvkSrQ7dtmXI130_head.
- NP210833.RA0sgjN1LIwyj_7qzNxQq5zmvjRrc6xjzSvkSrQ7dtmXI130_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." NP210833.RA0sgjN1LIwyj_7qzNxQq5zmvjRrc6xjzSvkSrQ7dtmXI130_provenance.
- NP210833.RA0sgjN1LIwyj_7qzNxQq5zmvjRrc6xjzSvkSrQ7dtmXI130_assertion evidence source_evidence_literature NP210833.RA0sgjN1LIwyj_7qzNxQq5zmvjRrc6xjzSvkSrQ7dtmXI130_provenance.
- NP210833.RA0sgjN1LIwyj_7qzNxQq5zmvjRrc6xjzSvkSrQ7dtmXI130_assertion SIO_000772 17613295 NP210833.RA0sgjN1LIwyj_7qzNxQq5zmvjRrc6xjzSvkSrQ7dtmXI130_provenance.
- NP210833.RA0sgjN1LIwyj_7qzNxQq5zmvjRrc6xjzSvkSrQ7dtmXI130_assertion wasDerivedFrom lhgdn-20090331 NP210833.RA0sgjN1LIwyj_7qzNxQq5zmvjRrc6xjzSvkSrQ7dtmXI130_provenance.
- NP210833.RA0sgjN1LIwyj_7qzNxQq5zmvjRrc6xjzSvkSrQ7dtmXI130_assertion wasGeneratedBy ECO_0000203 NP210833.RA0sgjN1LIwyj_7qzNxQq5zmvjRrc6xjzSvkSrQ7dtmXI130_provenance.