Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP775229.RAiNSsDMStHbfO5KBOkD8sXUxCwMuZNNSwSMGl7gv94GE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP775229.RAiNSsDMStHbfO5KBOkD8sXUxCwMuZNNSwSMGl7gv94GE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP775229.RAiNSsDMStHbfO5KBOkD8sXUxCwMuZNNSwSMGl7gv94GE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP775229.RAiNSsDMStHbfO5KBOkD8sXUxCwMuZNNSwSMGl7gv94GE130_provenance.
- NP775229.RAiNSsDMStHbfO5KBOkD8sXUxCwMuZNNSwSMGl7gv94GE130_assertion description "[However, the recent documentation of abnormal elevation of FMR1 mRNA, discovery of fragile X-associated tremor/ataxia syndrome (FXTAS), and reports of psychiatric disorders in children and adults with the premutation have suggested a pathogenic gene-brain-behavior mechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775229.RAiNSsDMStHbfO5KBOkD8sXUxCwMuZNNSwSMGl7gv94GE130_provenance.
- NP775229.RAiNSsDMStHbfO5KBOkD8sXUxCwMuZNNSwSMGl7gv94GE130_assertion evidence source_evidence_literature NP775229.RAiNSsDMStHbfO5KBOkD8sXUxCwMuZNNSwSMGl7gv94GE130_provenance.
- NP775229.RAiNSsDMStHbfO5KBOkD8sXUxCwMuZNNSwSMGl7gv94GE130_assertion SIO_000772 16184602 NP775229.RAiNSsDMStHbfO5KBOkD8sXUxCwMuZNNSwSMGl7gv94GE130_provenance.
- NP775229.RAiNSsDMStHbfO5KBOkD8sXUxCwMuZNNSwSMGl7gv94GE130_assertion wasDerivedFrom befree-20140225 NP775229.RAiNSsDMStHbfO5KBOkD8sXUxCwMuZNNSwSMGl7gv94GE130_provenance.
- NP775229.RAiNSsDMStHbfO5KBOkD8sXUxCwMuZNNSwSMGl7gv94GE130_assertion wasGeneratedBy ECO_0000203 NP775229.RAiNSsDMStHbfO5KBOkD8sXUxCwMuZNNSwSMGl7gv94GE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP775229.RAiNSsDMStHbfO5KBOkD8sXUxCwMuZNNSwSMGl7gv94GE130_provenance.