Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP789794.RABuMgW4MAz2Nv3EE5ZnYck4G-0jLzl7vdT-3r2zSoYSc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP789794.RABuMgW4MAz2Nv3EE5ZnYck4G-0jLzl7vdT-3r2zSoYSc130_assertion type Assertion NP789794.RABuMgW4MAz2Nv3EE5ZnYck4G-0jLzl7vdT-3r2zSoYSc130_head.
- NP789794.RABuMgW4MAz2Nv3EE5ZnYck4G-0jLzl7vdT-3r2zSoYSc130_assertion wasGeneratedBy ECO_0000203 NP789794.RABuMgW4MAz2Nv3EE5ZnYck4G-0jLzl7vdT-3r2zSoYSc130_provenance.
- NP789794.RABuMgW4MAz2Nv3EE5ZnYck4G-0jLzl7vdT-3r2zSoYSc130_assertion wasDerivedFrom befree-20150227 NP789794.RABuMgW4MAz2Nv3EE5ZnYck4G-0jLzl7vdT-3r2zSoYSc130_provenance.
- NP789794.RABuMgW4MAz2Nv3EE5ZnYck4G-0jLzl7vdT-3r2zSoYSc130_assertion SIO_000772 21658225 NP789794.RABuMgW4MAz2Nv3EE5ZnYck4G-0jLzl7vdT-3r2zSoYSc130_provenance.
- NP789794.RABuMgW4MAz2Nv3EE5ZnYck4G-0jLzl7vdT-3r2zSoYSc130_assertion evidence source_evidence_literature NP789794.RABuMgW4MAz2Nv3EE5ZnYck4G-0jLzl7vdT-3r2zSoYSc130_provenance.
- NP789794.RABuMgW4MAz2Nv3EE5ZnYck4G-0jLzl7vdT-3r2zSoYSc130_assertion description "[The identification of a large spectrum of MLL2 mutations possibly offers the opportunity to improve the actual knowledge on the clinical basis of this multiple congenital anomalies/mental retardation syndrome, design functional studies to understand the molecular mechanisms underlying this disease, establish genotype-phenotype correlations and improve clinical management.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789794.RABuMgW4MAz2Nv3EE5ZnYck4G-0jLzl7vdT-3r2zSoYSc130_provenance.