Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_provenance.
- NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_assertion description "[In order to evaluate the frequency of ARX mutation in XLMR, we performed mutational analysis of ARX in 165 mentally retarded probands negative for FRAXA and belonging to families in which the condition segregates as an X-linked condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_provenance.
- NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_assertion evidence source_evidence_literature NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_provenance.
- NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_assertion SIO_000772 16523516 NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_provenance.
- NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_assertion wasDerivedFrom befree-20140225 NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_provenance.
- NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_assertion wasGeneratedBy ECO_0000203 NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP743442.RAO72lzIRF5LbH0BJgXfur1AfgIqXVbj_exGiGJTJu5nY130_provenance.