Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP189387.RAnCxZtXeML95PaeuHol2vBVa12az13DdyG8fw5FZnflE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP189387.RAnCxZtXeML95PaeuHol2vBVa12az13DdyG8fw5FZnflE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP189387.RAnCxZtXeML95PaeuHol2vBVa12az13DdyG8fw5FZnflE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP189387.RAnCxZtXeML95PaeuHol2vBVa12az13DdyG8fw5FZnflE130_provenance.
- NP189387.RAnCxZtXeML95PaeuHol2vBVa12az13DdyG8fw5FZnflE130_assertion description "[Mutations in the ATR-X gene (ATRX) that encodes a putative global transcription factor have been identified in patients with ATR-X as well as those with other forms of X-linked mental retardation syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189387.RAnCxZtXeML95PaeuHol2vBVa12az13DdyG8fw5FZnflE130_provenance.
- NP189387.RAnCxZtXeML95PaeuHol2vBVa12az13DdyG8fw5FZnflE130_assertion evidence source_evidence_literature NP189387.RAnCxZtXeML95PaeuHol2vBVa12az13DdyG8fw5FZnflE130_provenance.
- NP189387.RAnCxZtXeML95PaeuHol2vBVa12az13DdyG8fw5FZnflE130_assertion SIO_000772 10995512 NP189387.RAnCxZtXeML95PaeuHol2vBVa12az13DdyG8fw5FZnflE130_provenance.
- NP189387.RAnCxZtXeML95PaeuHol2vBVa12az13DdyG8fw5FZnflE130_assertion wasDerivedFrom befree-20140225 NP189387.RAnCxZtXeML95PaeuHol2vBVa12az13DdyG8fw5FZnflE130_provenance.
- NP189387.RAnCxZtXeML95PaeuHol2vBVa12az13DdyG8fw5FZnflE130_assertion wasGeneratedBy ECO_0000203 NP189387.RAnCxZtXeML95PaeuHol2vBVa12az13DdyG8fw5FZnflE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP189387.RAnCxZtXeML95PaeuHol2vBVa12az13DdyG8fw5FZnflE130_provenance.