Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_assertion type Assertion NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_head.
- NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_assertion description "[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_provenance.
- NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_assertion evidence source_evidence_literature NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_provenance.
- NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_assertion SIO_000772 17262171 NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_provenance.
- NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_assertion wasDerivedFrom befree-20140225 NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_provenance.
- NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_assertion wasGeneratedBy ECO_0000203 NP186683.RAohMVHIAk_Kku_7HBgxUIn8DP0Mu2vYEqOiEetQOAuvs130_provenance.