Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP783251.RANS-sdJldU-J5emHsPmrxOlMdrtDk53t3fQuBHICJF4E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783251.RANS-sdJldU-J5emHsPmrxOlMdrtDk53t3fQuBHICJF4E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783251.RANS-sdJldU-J5emHsPmrxOlMdrtDk53t3fQuBHICJF4E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783251.RANS-sdJldU-J5emHsPmrxOlMdrtDk53t3fQuBHICJF4E130_provenance.
- NP783251.RANS-sdJldU-J5emHsPmrxOlMdrtDk53t3fQuBHICJF4E130_assertion description "[Our finding that disruption of PHF21A by translocations in the PSS region is associated with ID adds to the growing list of ID-associated genes that emphasize the critical role of transcriptional regulation and chromatin remodeling in normal brain development and cognitive function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783251.RANS-sdJldU-J5emHsPmrxOlMdrtDk53t3fQuBHICJF4E130_provenance.
- NP783251.RANS-sdJldU-J5emHsPmrxOlMdrtDk53t3fQuBHICJF4E130_assertion evidence source_evidence_literature NP783251.RANS-sdJldU-J5emHsPmrxOlMdrtDk53t3fQuBHICJF4E130_provenance.
- NP783251.RANS-sdJldU-J5emHsPmrxOlMdrtDk53t3fQuBHICJF4E130_assertion SIO_000772 22770980 NP783251.RANS-sdJldU-J5emHsPmrxOlMdrtDk53t3fQuBHICJF4E130_provenance.
- NP783251.RANS-sdJldU-J5emHsPmrxOlMdrtDk53t3fQuBHICJF4E130_assertion wasDerivedFrom befree-20140225 NP783251.RANS-sdJldU-J5emHsPmrxOlMdrtDk53t3fQuBHICJF4E130_provenance.
- NP783251.RANS-sdJldU-J5emHsPmrxOlMdrtDk53t3fQuBHICJF4E130_assertion wasGeneratedBy ECO_0000203 NP783251.RANS-sdJldU-J5emHsPmrxOlMdrtDk53t3fQuBHICJF4E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP783251.RANS-sdJldU-J5emHsPmrxOlMdrtDk53t3fQuBHICJF4E130_provenance.