Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP591319.RAdgGVb_cJpYPmpPxiFW-1O5VofD8qoJNPM_3fW8nJuCk130_assertion> ?p ?o ?g. }
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- NP591319.RAdgGVb_cJpYPmpPxiFW-1O5VofD8qoJNPM_3fW8nJuCk130_assertion type Assertion NP591319.RAdgGVb_cJpYPmpPxiFW-1O5VofD8qoJNPM_3fW8nJuCk130_head.
- NP591319.RAdgGVb_cJpYPmpPxiFW-1O5VofD8qoJNPM_3fW8nJuCk130_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." NP591319.RAdgGVb_cJpYPmpPxiFW-1O5VofD8qoJNPM_3fW8nJuCk130_provenance.
- NP591319.RAdgGVb_cJpYPmpPxiFW-1O5VofD8qoJNPM_3fW8nJuCk130_assertion evidence source_evidence_literature NP591319.RAdgGVb_cJpYPmpPxiFW-1O5VofD8qoJNPM_3fW8nJuCk130_provenance.
- NP591319.RAdgGVb_cJpYPmpPxiFW-1O5VofD8qoJNPM_3fW8nJuCk130_assertion SIO_000772 17262171 NP591319.RAdgGVb_cJpYPmpPxiFW-1O5VofD8qoJNPM_3fW8nJuCk130_provenance.
- NP591319.RAdgGVb_cJpYPmpPxiFW-1O5VofD8qoJNPM_3fW8nJuCk130_assertion wasDerivedFrom befree-2016 NP591319.RAdgGVb_cJpYPmpPxiFW-1O5VofD8qoJNPM_3fW8nJuCk130_provenance.
- NP591319.RAdgGVb_cJpYPmpPxiFW-1O5VofD8qoJNPM_3fW8nJuCk130_assertion wasGeneratedBy ECO_0000203 NP591319.RAdgGVb_cJpYPmpPxiFW-1O5VofD8qoJNPM_3fW8nJuCk130_provenance.