Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP983486.RAyd9ccIk2SHh7DsWMmaXOSBmURZppfwafbsXc0D9o8pA130_assertion> ?p ?o ?g. }
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- NP983486.RAyd9ccIk2SHh7DsWMmaXOSBmURZppfwafbsXc0D9o8pA130_assertion type Assertion NP983486.RAyd9ccIk2SHh7DsWMmaXOSBmURZppfwafbsXc0D9o8pA130_head.
- NP983486.RAyd9ccIk2SHh7DsWMmaXOSBmURZppfwafbsXc0D9o8pA130_assertion description "[Six patients with the diagnosis of both complete or segmental UPD including Prader-Willi syndrome (PWS; matUPD15), Angelman syndrome (AS; patUPD15), Silver-Russell syndrome (SRS; matUPD7), Beckwith-Wiedemann syndrome (BWS; patUPD11p), pseudohypoparathyroidism (PHP; patUPD20q) and a rare chromosomal rearrangement (patUPD2p, matUPD2q), were genotyped using the GeneChip Human Mapping 10K Array.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP983486.RAyd9ccIk2SHh7DsWMmaXOSBmURZppfwafbsXc0D9o8pA130_provenance.
- NP983486.RAyd9ccIk2SHh7DsWMmaXOSBmURZppfwafbsXc0D9o8pA130_assertion evidence source_evidence_literature NP983486.RAyd9ccIk2SHh7DsWMmaXOSBmURZppfwafbsXc0D9o8pA130_provenance.
- NP983486.RAyd9ccIk2SHh7DsWMmaXOSBmURZppfwafbsXc0D9o8pA130_assertion SIO_000772 15968682 NP983486.RAyd9ccIk2SHh7DsWMmaXOSBmURZppfwafbsXc0D9o8pA130_provenance.
- NP983486.RAyd9ccIk2SHh7DsWMmaXOSBmURZppfwafbsXc0D9o8pA130_assertion wasDerivedFrom befree-20150227 NP983486.RAyd9ccIk2SHh7DsWMmaXOSBmURZppfwafbsXc0D9o8pA130_provenance.
- NP983486.RAyd9ccIk2SHh7DsWMmaXOSBmURZppfwafbsXc0D9o8pA130_assertion wasGeneratedBy ECO_0000203 NP983486.RAyd9ccIk2SHh7DsWMmaXOSBmURZppfwafbsXc0D9o8pA130_provenance.