Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP539906.RA4AijR8DutoxwEhg7Lqv4PzTSLTFHRZaFslb92Vzp6Bw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP539906.RA4AijR8DutoxwEhg7Lqv4PzTSLTFHRZaFslb92Vzp6Bw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP539906.RA4AijR8DutoxwEhg7Lqv4PzTSLTFHRZaFslb92Vzp6Bw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP539906.RA4AijR8DutoxwEhg7Lqv4PzTSLTFHRZaFslb92Vzp6Bw130_provenance.
- NP539906.RA4AijR8DutoxwEhg7Lqv4PzTSLTFHRZaFslb92Vzp6Bw130_assertion description "[In addition to the results demonstrating the involvement of MECP2 in MRX, this study shows that the frequency of mutations in MECP2 in the mentally retarded population screened for the fragile X syndrome is comparable to the frequency of the CGG expansions in FMR1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539906.RA4AijR8DutoxwEhg7Lqv4PzTSLTFHRZaFslb92Vzp6Bw130_provenance.
- NP539906.RA4AijR8DutoxwEhg7Lqv4PzTSLTFHRZaFslb92Vzp6Bw130_assertion evidence source_evidence_literature NP539906.RA4AijR8DutoxwEhg7Lqv4PzTSLTFHRZaFslb92Vzp6Bw130_provenance.
- NP539906.RA4AijR8DutoxwEhg7Lqv4PzTSLTFHRZaFslb92Vzp6Bw130_assertion SIO_000772 11309367 NP539906.RA4AijR8DutoxwEhg7Lqv4PzTSLTFHRZaFslb92Vzp6Bw130_provenance.
- NP539906.RA4AijR8DutoxwEhg7Lqv4PzTSLTFHRZaFslb92Vzp6Bw130_assertion wasDerivedFrom befree-20140225 NP539906.RA4AijR8DutoxwEhg7Lqv4PzTSLTFHRZaFslb92Vzp6Bw130_provenance.
- NP539906.RA4AijR8DutoxwEhg7Lqv4PzTSLTFHRZaFslb92Vzp6Bw130_assertion wasGeneratedBy ECO_0000203 NP539906.RA4AijR8DutoxwEhg7Lqv4PzTSLTFHRZaFslb92Vzp6Bw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP539906.RA4AijR8DutoxwEhg7Lqv4PzTSLTFHRZaFslb92Vzp6Bw130_provenance.