Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP900718.RAgLGDQTkYcroCMIPtTJxGR6is3GHe30QzKSgLbF6Wltc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP900718.RAgLGDQTkYcroCMIPtTJxGR6is3GHe30QzKSgLbF6Wltc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP900718.RAgLGDQTkYcroCMIPtTJxGR6is3GHe30QzKSgLbF6Wltc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP900718.RAgLGDQTkYcroCMIPtTJxGR6is3GHe30QzKSgLbF6Wltc130_provenance.
- befree-2016 importedOn "2016-02-19" NP900718.RAgLGDQTkYcroCMIPtTJxGR6is3GHe30QzKSgLbF6Wltc130_provenance.
- NP900718.RAgLGDQTkYcroCMIPtTJxGR6is3GHe30QzKSgLbF6Wltc130_assertion wasGeneratedBy ECO_0000203 NP900718.RAgLGDQTkYcroCMIPtTJxGR6is3GHe30QzKSgLbF6Wltc130_provenance.
- NP900718.RAgLGDQTkYcroCMIPtTJxGR6is3GHe30QzKSgLbF6Wltc130_assertion wasDerivedFrom befree-2016 NP900718.RAgLGDQTkYcroCMIPtTJxGR6is3GHe30QzKSgLbF6Wltc130_provenance.
- NP900718.RAgLGDQTkYcroCMIPtTJxGR6is3GHe30QzKSgLbF6Wltc130_assertion SIO_000772 21658225 NP900718.RAgLGDQTkYcroCMIPtTJxGR6is3GHe30QzKSgLbF6Wltc130_provenance.
- NP900718.RAgLGDQTkYcroCMIPtTJxGR6is3GHe30QzKSgLbF6Wltc130_assertion evidence source_evidence_literature NP900718.RAgLGDQTkYcroCMIPtTJxGR6is3GHe30QzKSgLbF6Wltc130_provenance.
- NP900718.RAgLGDQTkYcroCMIPtTJxGR6is3GHe30QzKSgLbF6Wltc130_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." NP900718.RAgLGDQTkYcroCMIPtTJxGR6is3GHe30QzKSgLbF6Wltc130_provenance.