Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP304402.RApWsS9XUliBhdxAZfqnGQeWWycxjXbJxdB2KvbKvs-YA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP304402.RApWsS9XUliBhdxAZfqnGQeWWycxjXbJxdB2KvbKvs-YA130_assertion type Assertion NP304402.RApWsS9XUliBhdxAZfqnGQeWWycxjXbJxdB2KvbKvs-YA130_head.
- NP304402.RApWsS9XUliBhdxAZfqnGQeWWycxjXbJxdB2KvbKvs-YA130_assertion wasGeneratedBy ECO_0000203 NP304402.RApWsS9XUliBhdxAZfqnGQeWWycxjXbJxdB2KvbKvs-YA130_provenance.
- NP304402.RApWsS9XUliBhdxAZfqnGQeWWycxjXbJxdB2KvbKvs-YA130_assertion wasDerivedFrom befree-20140225 NP304402.RApWsS9XUliBhdxAZfqnGQeWWycxjXbJxdB2KvbKvs-YA130_provenance.
- NP304402.RApWsS9XUliBhdxAZfqnGQeWWycxjXbJxdB2KvbKvs-YA130_assertion SIO_000772 10451515 NP304402.RApWsS9XUliBhdxAZfqnGQeWWycxjXbJxdB2KvbKvs-YA130_provenance.
- NP304402.RApWsS9XUliBhdxAZfqnGQeWWycxjXbJxdB2KvbKvs-YA130_assertion evidence source_evidence_literature NP304402.RApWsS9XUliBhdxAZfqnGQeWWycxjXbJxdB2KvbKvs-YA130_provenance.
- NP304402.RApWsS9XUliBhdxAZfqnGQeWWycxjXbJxdB2KvbKvs-YA130_assertion description "[Because SMC(15) were found at an increased incidence in patients with PWS/AS, we performed methylation analysis at the SNRPN locus to exclude a deletion or uniparental disomy (UPD) of chromosome 15.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP304402.RApWsS9XUliBhdxAZfqnGQeWWycxjXbJxdB2KvbKvs-YA130_provenance.