Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP569091.RAkhFIx1-11lYku7mAxyFtY6096-dH52NlpqcDmEymnVc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP569091.RAkhFIx1-11lYku7mAxyFtY6096-dH52NlpqcDmEymnVc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569091.RAkhFIx1-11lYku7mAxyFtY6096-dH52NlpqcDmEymnVc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569091.RAkhFIx1-11lYku7mAxyFtY6096-dH52NlpqcDmEymnVc130_provenance.
- NP569091.RAkhFIx1-11lYku7mAxyFtY6096-dH52NlpqcDmEymnVc130_assertion description "[About 30% of the mutations causing nonsyndromic X-linked mental retardation (MRX) are thought to be located in Xp11 and in the pericentromeric region, with a particular clustering of gene defects in a 7.4 Mb interval flanked by the genes ELK1 and ALAS2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569091.RAkhFIx1-11lYku7mAxyFtY6096-dH52NlpqcDmEymnVc130_provenance.
- NP569091.RAkhFIx1-11lYku7mAxyFtY6096-dH52NlpqcDmEymnVc130_assertion evidence source_evidence_literature NP569091.RAkhFIx1-11lYku7mAxyFtY6096-dH52NlpqcDmEymnVc130_provenance.
- NP569091.RAkhFIx1-11lYku7mAxyFtY6096-dH52NlpqcDmEymnVc130_assertion SIO_000772 16969374 NP569091.RAkhFIx1-11lYku7mAxyFtY6096-dH52NlpqcDmEymnVc130_provenance.
- NP569091.RAkhFIx1-11lYku7mAxyFtY6096-dH52NlpqcDmEymnVc130_assertion wasDerivedFrom befree-2016 NP569091.RAkhFIx1-11lYku7mAxyFtY6096-dH52NlpqcDmEymnVc130_provenance.
- NP569091.RAkhFIx1-11lYku7mAxyFtY6096-dH52NlpqcDmEymnVc130_assertion wasGeneratedBy ECO_0000203 NP569091.RAkhFIx1-11lYku7mAxyFtY6096-dH52NlpqcDmEymnVc130_provenance.
- befree-2016 importedOn "2016-02-19" NP569091.RAkhFIx1-11lYku7mAxyFtY6096-dH52NlpqcDmEymnVc130_provenance.