Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP415844.RAXZWRJITGCX0IC1r-_wf49bfBtDIv-LN5v_Jgg3UAJf8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP415844.RAXZWRJITGCX0IC1r-_wf49bfBtDIv-LN5v_Jgg3UAJf8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP415844.RAXZWRJITGCX0IC1r-_wf49bfBtDIv-LN5v_Jgg3UAJf8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP415844.RAXZWRJITGCX0IC1r-_wf49bfBtDIv-LN5v_Jgg3UAJf8130_provenance.
- NP415844.RAXZWRJITGCX0IC1r-_wf49bfBtDIv-LN5v_Jgg3UAJf8130_assertion description "[These results define an epigenotype-phenotype relationship in BWS, in which aberrant methylation of H19 and LIT1 and UPD are strongly associated with cancer risk and specific birth defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP415844.RAXZWRJITGCX0IC1r-_wf49bfBtDIv-LN5v_Jgg3UAJf8130_provenance.
- NP415844.RAXZWRJITGCX0IC1r-_wf49bfBtDIv-LN5v_Jgg3UAJf8130_assertion evidence source_evidence_literature NP415844.RAXZWRJITGCX0IC1r-_wf49bfBtDIv-LN5v_Jgg3UAJf8130_provenance.
- NP415844.RAXZWRJITGCX0IC1r-_wf49bfBtDIv-LN5v_Jgg3UAJf8130_assertion SIO_000772 11813134 NP415844.RAXZWRJITGCX0IC1r-_wf49bfBtDIv-LN5v_Jgg3UAJf8130_provenance.
- NP415844.RAXZWRJITGCX0IC1r-_wf49bfBtDIv-LN5v_Jgg3UAJf8130_assertion wasDerivedFrom befree-20140225 NP415844.RAXZWRJITGCX0IC1r-_wf49bfBtDIv-LN5v_Jgg3UAJf8130_provenance.
- NP415844.RAXZWRJITGCX0IC1r-_wf49bfBtDIv-LN5v_Jgg3UAJf8130_assertion wasGeneratedBy ECO_0000203 NP415844.RAXZWRJITGCX0IC1r-_wf49bfBtDIv-LN5v_Jgg3UAJf8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP415844.RAXZWRJITGCX0IC1r-_wf49bfBtDIv-LN5v_Jgg3UAJf8130_provenance.