Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP900715.RAbim6krmtpb9C_3-Mxk0YzKD4ymNvgQUsqln0UZsj--c130_assertion> ?p ?o ?g. }
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- NP900715.RAbim6krmtpb9C_3-Mxk0YzKD4ymNvgQUsqln0UZsj--c130_assertion type Assertion NP900715.RAbim6krmtpb9C_3-Mxk0YzKD4ymNvgQUsqln0UZsj--c130_head.
- NP900715.RAbim6krmtpb9C_3-Mxk0YzKD4ymNvgQUsqln0UZsj--c130_assertion wasGeneratedBy ECO_0000203 NP900715.RAbim6krmtpb9C_3-Mxk0YzKD4ymNvgQUsqln0UZsj--c130_provenance.
- NP900715.RAbim6krmtpb9C_3-Mxk0YzKD4ymNvgQUsqln0UZsj--c130_assertion wasDerivedFrom befree-2016 NP900715.RAbim6krmtpb9C_3-Mxk0YzKD4ymNvgQUsqln0UZsj--c130_provenance.
- NP900715.RAbim6krmtpb9C_3-Mxk0YzKD4ymNvgQUsqln0UZsj--c130_assertion SIO_000772 21658225 NP900715.RAbim6krmtpb9C_3-Mxk0YzKD4ymNvgQUsqln0UZsj--c130_provenance.
- NP900715.RAbim6krmtpb9C_3-Mxk0YzKD4ymNvgQUsqln0UZsj--c130_assertion evidence source_evidence_literature NP900715.RAbim6krmtpb9C_3-Mxk0YzKD4ymNvgQUsqln0UZsj--c130_provenance.
- NP900715.RAbim6krmtpb9C_3-Mxk0YzKD4ymNvgQUsqln0UZsj--c130_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." NP900715.RAbim6krmtpb9C_3-Mxk0YzKD4ymNvgQUsqln0UZsj--c130_provenance.