Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP658065.RADMGlbp7FmYXWkCUxZ58t2qp1_MKLEiPAMVt6t67xRr4130_assertion> ?p ?o ?g. }
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- NP658065.RADMGlbp7FmYXWkCUxZ58t2qp1_MKLEiPAMVt6t67xRr4130_assertion type Assertion NP658065.RADMGlbp7FmYXWkCUxZ58t2qp1_MKLEiPAMVt6t67xRr4130_head.
- NP658065.RADMGlbp7FmYXWkCUxZ58t2qp1_MKLEiPAMVt6t67xRr4130_assertion description "[Over the last decade it has become increasingly clear that mutations of genes involved in epigenetic mechanism, such as DNA methyltransferases, methyl-binding domain proteins, histone deacetylases, histone methylases and members of the SWI/SNF family of chromatin remodelers are linked to human disorders, including Immunodeficiency Centromeric instability Facial syndrome 1, Rett syndrome, Rubinstein-Taybi syndrome, Sotos syndrome or alpha-thalassemia/mental retardation X-linked syndrome, among others.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658065.RADMGlbp7FmYXWkCUxZ58t2qp1_MKLEiPAMVt6t67xRr4130_provenance.
- NP658065.RADMGlbp7FmYXWkCUxZ58t2qp1_MKLEiPAMVt6t67xRr4130_assertion evidence source_evidence_literature NP658065.RADMGlbp7FmYXWkCUxZ58t2qp1_MKLEiPAMVt6t67xRr4130_provenance.
- NP658065.RADMGlbp7FmYXWkCUxZ58t2qp1_MKLEiPAMVt6t67xRr4130_assertion SIO_000772 23370504 NP658065.RADMGlbp7FmYXWkCUxZ58t2qp1_MKLEiPAMVt6t67xRr4130_provenance.
- NP658065.RADMGlbp7FmYXWkCUxZ58t2qp1_MKLEiPAMVt6t67xRr4130_assertion wasDerivedFrom befree-20140225 NP658065.RADMGlbp7FmYXWkCUxZ58t2qp1_MKLEiPAMVt6t67xRr4130_provenance.
- NP658065.RADMGlbp7FmYXWkCUxZ58t2qp1_MKLEiPAMVt6t67xRr4130_assertion wasGeneratedBy ECO_0000203 NP658065.RADMGlbp7FmYXWkCUxZ58t2qp1_MKLEiPAMVt6t67xRr4130_provenance.