Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP500362.RAa2kMhT69e_c2Jh0Ia-4T2oK4rGiNwX_mmIEz3-2YzrQ130_assertion> ?p ?o ?g. }
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- NP500362.RAa2kMhT69e_c2Jh0Ia-4T2oK4rGiNwX_mmIEz3-2YzrQ130_assertion type Assertion NP500362.RAa2kMhT69e_c2Jh0Ia-4T2oK4rGiNwX_mmIEz3-2YzrQ130_head.
- NP500362.RAa2kMhT69e_c2Jh0Ia-4T2oK4rGiNwX_mmIEz3-2YzrQ130_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." NP500362.RAa2kMhT69e_c2Jh0Ia-4T2oK4rGiNwX_mmIEz3-2YzrQ130_provenance.
- NP500362.RAa2kMhT69e_c2Jh0Ia-4T2oK4rGiNwX_mmIEz3-2YzrQ130_assertion evidence source_evidence_literature NP500362.RAa2kMhT69e_c2Jh0Ia-4T2oK4rGiNwX_mmIEz3-2YzrQ130_provenance.
- NP500362.RAa2kMhT69e_c2Jh0Ia-4T2oK4rGiNwX_mmIEz3-2YzrQ130_assertion SIO_000772 15968682 NP500362.RAa2kMhT69e_c2Jh0Ia-4T2oK4rGiNwX_mmIEz3-2YzrQ130_provenance.
- NP500362.RAa2kMhT69e_c2Jh0Ia-4T2oK4rGiNwX_mmIEz3-2YzrQ130_assertion wasDerivedFrom befree-2016 NP500362.RAa2kMhT69e_c2Jh0Ia-4T2oK4rGiNwX_mmIEz3-2YzrQ130_provenance.
- NP500362.RAa2kMhT69e_c2Jh0Ia-4T2oK4rGiNwX_mmIEz3-2YzrQ130_assertion wasGeneratedBy ECO_0000203 NP500362.RAa2kMhT69e_c2Jh0Ia-4T2oK4rGiNwX_mmIEz3-2YzrQ130_provenance.