Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP619628.RA-3Y0wkiLctyRbF0SWkI4Bxs13W2nmB7dhsWFUDgV0ZQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP619628.RA-3Y0wkiLctyRbF0SWkI4Bxs13W2nmB7dhsWFUDgV0ZQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP619628.RA-3Y0wkiLctyRbF0SWkI4Bxs13W2nmB7dhsWFUDgV0ZQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP619628.RA-3Y0wkiLctyRbF0SWkI4Bxs13W2nmB7dhsWFUDgV0ZQ130_provenance.
- NP619628.RA-3Y0wkiLctyRbF0SWkI4Bxs13W2nmB7dhsWFUDgV0ZQ130_assertion description "[In particular, these include significantly reduced expression levels of three matrix metallopeptidases (MMP1, MMP3, MMP16), follistatin, and STAT1, and significantly increased expression levels of fibroblast growth factors (FGF9, FGF11), a number of collagen genes and other ECM genes in DD patient samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619628.RA-3Y0wkiLctyRbF0SWkI4Bxs13W2nmB7dhsWFUDgV0ZQ130_provenance.
- NP619628.RA-3Y0wkiLctyRbF0SWkI4Bxs13W2nmB7dhsWFUDgV0ZQ130_assertion evidence source_evidence_literature NP619628.RA-3Y0wkiLctyRbF0SWkI4Bxs13W2nmB7dhsWFUDgV0ZQ130_provenance.
- NP619628.RA-3Y0wkiLctyRbF0SWkI4Bxs13W2nmB7dhsWFUDgV0ZQ130_assertion SIO_000772 23554969 NP619628.RA-3Y0wkiLctyRbF0SWkI4Bxs13W2nmB7dhsWFUDgV0ZQ130_provenance.
- NP619628.RA-3Y0wkiLctyRbF0SWkI4Bxs13W2nmB7dhsWFUDgV0ZQ130_assertion wasDerivedFrom befree-20140225 NP619628.RA-3Y0wkiLctyRbF0SWkI4Bxs13W2nmB7dhsWFUDgV0ZQ130_provenance.
- NP619628.RA-3Y0wkiLctyRbF0SWkI4Bxs13W2nmB7dhsWFUDgV0ZQ130_assertion wasGeneratedBy ECO_0000203 NP619628.RA-3Y0wkiLctyRbF0SWkI4Bxs13W2nmB7dhsWFUDgV0ZQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP619628.RA-3Y0wkiLctyRbF0SWkI4Bxs13W2nmB7dhsWFUDgV0ZQ130_provenance.