Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP829958.RAjkFtSPUP1_tqhbSWjPjJF9sV5wVFYvFd1ENewSsRMnw130_assertion> ?p ?o ?g. }
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- NP829958.RAjkFtSPUP1_tqhbSWjPjJF9sV5wVFYvFd1ENewSsRMnw130_assertion type Assertion NP829958.RAjkFtSPUP1_tqhbSWjPjJF9sV5wVFYvFd1ENewSsRMnw130_head.
- NP829958.RAjkFtSPUP1_tqhbSWjPjJF9sV5wVFYvFd1ENewSsRMnw130_assertion wasGeneratedBy ECO_0000203 NP829958.RAjkFtSPUP1_tqhbSWjPjJF9sV5wVFYvFd1ENewSsRMnw130_provenance.
- NP829958.RAjkFtSPUP1_tqhbSWjPjJF9sV5wVFYvFd1ENewSsRMnw130_assertion wasDerivedFrom befree-20150227 NP829958.RAjkFtSPUP1_tqhbSWjPjJF9sV5wVFYvFd1ENewSsRMnw130_provenance.
- NP829958.RAjkFtSPUP1_tqhbSWjPjJF9sV5wVFYvFd1ENewSsRMnw130_assertion SIO_000772 21658225 NP829958.RAjkFtSPUP1_tqhbSWjPjJF9sV5wVFYvFd1ENewSsRMnw130_provenance.
- NP829958.RAjkFtSPUP1_tqhbSWjPjJF9sV5wVFYvFd1ENewSsRMnw130_assertion evidence source_evidence_literature NP829958.RAjkFtSPUP1_tqhbSWjPjJF9sV5wVFYvFd1ENewSsRMnw130_provenance.
- NP829958.RAjkFtSPUP1_tqhbSWjPjJF9sV5wVFYvFd1ENewSsRMnw130_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." NP829958.RAjkFtSPUP1_tqhbSWjPjJF9sV5wVFYvFd1ENewSsRMnw130_provenance.