Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_assertion type Assertion NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_head.
- NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_assertion description "[We report two unrelated patients with MWS where the clinical diagnosis was established only after finding of disruption of the ZEB2 gene by a balanced translocation breakpoint and an interstitial microdeletion, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_provenance.
- NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_assertion evidence source_evidence_literature NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_provenance.
- NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_assertion SIO_000772 18445050 NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_provenance.
- NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_assertion wasDerivedFrom befree-20150227 NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_provenance.
- NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_assertion wasGeneratedBy ECO_0000203 NP831179.RAd55htfT-Sz8pUib6k5TeECN_GjLOAJPOja0Enme119Q130_provenance.