Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP518629.RAEqBTERMr5KTKx0N54K4eAIev2nsF0yXVOCR4aZQMGeU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP518629.RAEqBTERMr5KTKx0N54K4eAIev2nsF0yXVOCR4aZQMGeU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP518629.RAEqBTERMr5KTKx0N54K4eAIev2nsF0yXVOCR4aZQMGeU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP518629.RAEqBTERMr5KTKx0N54K4eAIev2nsF0yXVOCR4aZQMGeU130_provenance.
- NP518629.RAEqBTERMr5KTKx0N54K4eAIev2nsF0yXVOCR4aZQMGeU130_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." NP518629.RAEqBTERMr5KTKx0N54K4eAIev2nsF0yXVOCR4aZQMGeU130_provenance.
- NP518629.RAEqBTERMr5KTKx0N54K4eAIev2nsF0yXVOCR4aZQMGeU130_assertion evidence source_evidence_literature NP518629.RAEqBTERMr5KTKx0N54K4eAIev2nsF0yXVOCR4aZQMGeU130_provenance.
- NP518629.RAEqBTERMr5KTKx0N54K4eAIev2nsF0yXVOCR4aZQMGeU130_assertion SIO_000772 16235064 NP518629.RAEqBTERMr5KTKx0N54K4eAIev2nsF0yXVOCR4aZQMGeU130_provenance.
- NP518629.RAEqBTERMr5KTKx0N54K4eAIev2nsF0yXVOCR4aZQMGeU130_assertion wasDerivedFrom befree-2016 NP518629.RAEqBTERMr5KTKx0N54K4eAIev2nsF0yXVOCR4aZQMGeU130_provenance.
- NP518629.RAEqBTERMr5KTKx0N54K4eAIev2nsF0yXVOCR4aZQMGeU130_assertion wasGeneratedBy ECO_0000203 NP518629.RAEqBTERMr5KTKx0N54K4eAIev2nsF0yXVOCR4aZQMGeU130_provenance.
- befree-2016 importedOn "2016-02-19" NP518629.RAEqBTERMr5KTKx0N54K4eAIev2nsF0yXVOCR4aZQMGeU130_provenance.