Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1035748.RAa84KrpO3M-1pphM6LyW4NPXsAGUVnuJc3mI4OstXfAA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1035748.RAa84KrpO3M-1pphM6LyW4NPXsAGUVnuJc3mI4OstXfAA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1035748.RAa84KrpO3M-1pphM6LyW4NPXsAGUVnuJc3mI4OstXfAA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1035748.RAa84KrpO3M-1pphM6LyW4NPXsAGUVnuJc3mI4OstXfAA130_provenance.
- NP1035748.RAa84KrpO3M-1pphM6LyW4NPXsAGUVnuJc3mI4OstXfAA130_assertion description "[The fragile X syndrome is a mutation-driven developmental disorder caused by a repetition over 200 times of the CGG trinucleotide situated in the 5'-untranslated region of the fragile X mental retardation 1 gene (FMR1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1035748.RAa84KrpO3M-1pphM6LyW4NPXsAGUVnuJc3mI4OstXfAA130_provenance.
- NP1035748.RAa84KrpO3M-1pphM6LyW4NPXsAGUVnuJc3mI4OstXfAA130_assertion evidence source_evidence_literature NP1035748.RAa84KrpO3M-1pphM6LyW4NPXsAGUVnuJc3mI4OstXfAA130_provenance.
- NP1035748.RAa84KrpO3M-1pphM6LyW4NPXsAGUVnuJc3mI4OstXfAA130_assertion SIO_000772 23236003 NP1035748.RAa84KrpO3M-1pphM6LyW4NPXsAGUVnuJc3mI4OstXfAA130_provenance.
- NP1035748.RAa84KrpO3M-1pphM6LyW4NPXsAGUVnuJc3mI4OstXfAA130_assertion wasDerivedFrom befree-2016 NP1035748.RAa84KrpO3M-1pphM6LyW4NPXsAGUVnuJc3mI4OstXfAA130_provenance.
- NP1035748.RAa84KrpO3M-1pphM6LyW4NPXsAGUVnuJc3mI4OstXfAA130_assertion wasGeneratedBy ECO_0000203 NP1035748.RAa84KrpO3M-1pphM6LyW4NPXsAGUVnuJc3mI4OstXfAA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1035748.RAa84KrpO3M-1pphM6LyW4NPXsAGUVnuJc3mI4OstXfAA130_provenance.