Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP743997.RAEE1Y60vdZ6WDlYOdnEDgZyvKiGN6TrVtS5oFPc3qf-o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP743997.RAEE1Y60vdZ6WDlYOdnEDgZyvKiGN6TrVtS5oFPc3qf-o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP743997.RAEE1Y60vdZ6WDlYOdnEDgZyvKiGN6TrVtS5oFPc3qf-o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP743997.RAEE1Y60vdZ6WDlYOdnEDgZyvKiGN6TrVtS5oFPc3qf-o130_provenance.
- NP743997.RAEE1Y60vdZ6WDlYOdnEDgZyvKiGN6TrVtS5oFPc3qf-o130_assertion wasGeneratedBy ECO_0000203 NP743997.RAEE1Y60vdZ6WDlYOdnEDgZyvKiGN6TrVtS5oFPc3qf-o130_provenance.
- NP743997.RAEE1Y60vdZ6WDlYOdnEDgZyvKiGN6TrVtS5oFPc3qf-o130_assertion wasDerivedFrom befree-20140225 NP743997.RAEE1Y60vdZ6WDlYOdnEDgZyvKiGN6TrVtS5oFPc3qf-o130_provenance.
- NP743997.RAEE1Y60vdZ6WDlYOdnEDgZyvKiGN6TrVtS5oFPc3qf-o130_assertion SIO_000772 11559911 NP743997.RAEE1Y60vdZ6WDlYOdnEDgZyvKiGN6TrVtS5oFPc3qf-o130_provenance.
- NP743997.RAEE1Y60vdZ6WDlYOdnEDgZyvKiGN6TrVtS5oFPc3qf-o130_assertion evidence source_evidence_literature NP743997.RAEE1Y60vdZ6WDlYOdnEDgZyvKiGN6TrVtS5oFPc3qf-o130_provenance.
- NP743997.RAEE1Y60vdZ6WDlYOdnEDgZyvKiGN6TrVtS5oFPc3qf-o130_assertion description "[Given that molecular investigation of XNP/ATR-X mutations is made onerous by the length of the gene transcript, we carried out a prenatal diagnosis in a fetus at risk for ATR-X syndrome by initially determining the XNP/ATR-X gene haplotype before considering gene sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743997.RAEE1Y60vdZ6WDlYOdnEDgZyvKiGN6TrVtS5oFPc3qf-o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP743997.RAEE1Y60vdZ6WDlYOdnEDgZyvKiGN6TrVtS5oFPc3qf-o130_provenance.