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- source_evidence_literature type ECO_0000212 NP978182.RAdDoQUkekmylz7fRbDAY47y09BQhjX6RCk75cgp5Vmcc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978182.RAdDoQUkekmylz7fRbDAY47y09BQhjX6RCk75cgp5Vmcc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978182.RAdDoQUkekmylz7fRbDAY47y09BQhjX6RCk75cgp5Vmcc130_provenance.
- NP978182.RAdDoQUkekmylz7fRbDAY47y09BQhjX6RCk75cgp5Vmcc130_assertion description "[This study confirms that the frequency of ARX mutations is high in XLMR, and the analysis of ARX in MRX should not be limited to duplication.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978182.RAdDoQUkekmylz7fRbDAY47y09BQhjX6RCk75cgp5Vmcc130_provenance.
- NP978182.RAdDoQUkekmylz7fRbDAY47y09BQhjX6RCk75cgp5Vmcc130_assertion evidence source_evidence_literature NP978182.RAdDoQUkekmylz7fRbDAY47y09BQhjX6RCk75cgp5Vmcc130_provenance.
- NP978182.RAdDoQUkekmylz7fRbDAY47y09BQhjX6RCk75cgp5Vmcc130_assertion SIO_000772 16235064 NP978182.RAdDoQUkekmylz7fRbDAY47y09BQhjX6RCk75cgp5Vmcc130_provenance.
- NP978182.RAdDoQUkekmylz7fRbDAY47y09BQhjX6RCk75cgp5Vmcc130_assertion wasDerivedFrom befree-20150227 NP978182.RAdDoQUkekmylz7fRbDAY47y09BQhjX6RCk75cgp5Vmcc130_provenance.
- NP978182.RAdDoQUkekmylz7fRbDAY47y09BQhjX6RCk75cgp5Vmcc130_assertion wasGeneratedBy ECO_0000203 NP978182.RAdDoQUkekmylz7fRbDAY47y09BQhjX6RCk75cgp5Vmcc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978182.RAdDoQUkekmylz7fRbDAY47y09BQhjX6RCk75cgp5Vmcc130_provenance.