Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP211552.RAfR_pnAE1Bm2cah_G4bxOsvfGPtD_xI6oMvb4vgoItKc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP211552.RAfR_pnAE1Bm2cah_G4bxOsvfGPtD_xI6oMvb4vgoItKc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP211552.RAfR_pnAE1Bm2cah_G4bxOsvfGPtD_xI6oMvb4vgoItKc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP211552.RAfR_pnAE1Bm2cah_G4bxOsvfGPtD_xI6oMvb4vgoItKc130_provenance.
- NP211552.RAfR_pnAE1Bm2cah_G4bxOsvfGPtD_xI6oMvb4vgoItKc130_assertion description "[The H19 gene is abundantly expressed by the human placenta and is implicated in the pathogenesis of congenital growth disorders such as Beckwith-Wiedemann (BWS) and Silver-Russell (SRS) syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211552.RAfR_pnAE1Bm2cah_G4bxOsvfGPtD_xI6oMvb4vgoItKc130_provenance.
- NP211552.RAfR_pnAE1Bm2cah_G4bxOsvfGPtD_xI6oMvb4vgoItKc130_assertion evidence source_evidence_literature NP211552.RAfR_pnAE1Bm2cah_G4bxOsvfGPtD_xI6oMvb4vgoItKc130_provenance.
- NP211552.RAfR_pnAE1Bm2cah_G4bxOsvfGPtD_xI6oMvb4vgoItKc130_assertion SIO_000772 21129773 NP211552.RAfR_pnAE1Bm2cah_G4bxOsvfGPtD_xI6oMvb4vgoItKc130_provenance.
- NP211552.RAfR_pnAE1Bm2cah_G4bxOsvfGPtD_xI6oMvb4vgoItKc130_assertion wasDerivedFrom befree-20140225 NP211552.RAfR_pnAE1Bm2cah_G4bxOsvfGPtD_xI6oMvb4vgoItKc130_provenance.
- NP211552.RAfR_pnAE1Bm2cah_G4bxOsvfGPtD_xI6oMvb4vgoItKc130_assertion wasGeneratedBy ECO_0000203 NP211552.RAfR_pnAE1Bm2cah_G4bxOsvfGPtD_xI6oMvb4vgoItKc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP211552.RAfR_pnAE1Bm2cah_G4bxOsvfGPtD_xI6oMvb4vgoItKc130_provenance.