Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP591320.RAtxhqxblzpbSg3LAIaeGDVHl8yG9c4IIAI1MCG4C12jg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP591320.RAtxhqxblzpbSg3LAIaeGDVHl8yG9c4IIAI1MCG4C12jg130_assertion type Assertion NP591320.RAtxhqxblzpbSg3LAIaeGDVHl8yG9c4IIAI1MCG4C12jg130_head.
- NP591320.RAtxhqxblzpbSg3LAIaeGDVHl8yG9c4IIAI1MCG4C12jg130_assertion description "[Analysis of candidate imprinted genes in PWS subjects with atypical genetics: a possible inactivating mutation in the SNURF/SNRPN minimal promoter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP591320.RAtxhqxblzpbSg3LAIaeGDVHl8yG9c4IIAI1MCG4C12jg130_provenance.
- NP591320.RAtxhqxblzpbSg3LAIaeGDVHl8yG9c4IIAI1MCG4C12jg130_assertion evidence source_evidence_literature NP591320.RAtxhqxblzpbSg3LAIaeGDVHl8yG9c4IIAI1MCG4C12jg130_provenance.
- NP591320.RAtxhqxblzpbSg3LAIaeGDVHl8yG9c4IIAI1MCG4C12jg130_assertion SIO_000772 17262171 NP591320.RAtxhqxblzpbSg3LAIaeGDVHl8yG9c4IIAI1MCG4C12jg130_provenance.
- NP591320.RAtxhqxblzpbSg3LAIaeGDVHl8yG9c4IIAI1MCG4C12jg130_assertion wasDerivedFrom befree-2016 NP591320.RAtxhqxblzpbSg3LAIaeGDVHl8yG9c4IIAI1MCG4C12jg130_provenance.
- NP591320.RAtxhqxblzpbSg3LAIaeGDVHl8yG9c4IIAI1MCG4C12jg130_assertion wasGeneratedBy ECO_0000203 NP591320.RAtxhqxblzpbSg3LAIaeGDVHl8yG9c4IIAI1MCG4C12jg130_provenance.