Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP249731.RAks0sVeZlRTlc0GRX_RdHlt0ccKUBMtEiLyPWAbsZ77s130_assertion> ?p ?o ?g. }
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- NP249731.RAks0sVeZlRTlc0GRX_RdHlt0ccKUBMtEiLyPWAbsZ77s130_assertion type Assertion NP249731.RAks0sVeZlRTlc0GRX_RdHlt0ccKUBMtEiLyPWAbsZ77s130_head.
- NP249731.RAks0sVeZlRTlc0GRX_RdHlt0ccKUBMtEiLyPWAbsZ77s130_assertion wasGeneratedBy ECO_0000203 NP249731.RAks0sVeZlRTlc0GRX_RdHlt0ccKUBMtEiLyPWAbsZ77s130_provenance.
- NP249731.RAks0sVeZlRTlc0GRX_RdHlt0ccKUBMtEiLyPWAbsZ77s130_assertion wasDerivedFrom befree-20140225 NP249731.RAks0sVeZlRTlc0GRX_RdHlt0ccKUBMtEiLyPWAbsZ77s130_provenance.
- NP249731.RAks0sVeZlRTlc0GRX_RdHlt0ccKUBMtEiLyPWAbsZ77s130_assertion SIO_000772 21658225 NP249731.RAks0sVeZlRTlc0GRX_RdHlt0ccKUBMtEiLyPWAbsZ77s130_provenance.
- NP249731.RAks0sVeZlRTlc0GRX_RdHlt0ccKUBMtEiLyPWAbsZ77s130_assertion evidence source_evidence_literature NP249731.RAks0sVeZlRTlc0GRX_RdHlt0ccKUBMtEiLyPWAbsZ77s130_provenance.
- NP249731.RAks0sVeZlRTlc0GRX_RdHlt0ccKUBMtEiLyPWAbsZ77s130_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." NP249731.RAks0sVeZlRTlc0GRX_RdHlt0ccKUBMtEiLyPWAbsZ77s130_provenance.