Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP470148.RAeitRrAFY6KiCnY5gsb6wXInB4cDlHMFtdsIB61DK9vA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP470148.RAeitRrAFY6KiCnY5gsb6wXInB4cDlHMFtdsIB61DK9vA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470148.RAeitRrAFY6KiCnY5gsb6wXInB4cDlHMFtdsIB61DK9vA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470148.RAeitRrAFY6KiCnY5gsb6wXInB4cDlHMFtdsIB61DK9vA130_provenance.
- NP470148.RAeitRrAFY6KiCnY5gsb6wXInB4cDlHMFtdsIB61DK9vA130_assertion description "[Recently, reports of the combined syndrome of JPS and HHT have been described in individuals with mutations in the SMAD4 gene, whose product-SMAD4-is a critical intracellular effector in the signalling pathway of transforming growth factor beta (TGFbeta).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470148.RAeitRrAFY6KiCnY5gsb6wXInB4cDlHMFtdsIB61DK9vA130_provenance.
- NP470148.RAeitRrAFY6KiCnY5gsb6wXInB4cDlHMFtdsIB61DK9vA130_assertion evidence source_evidence_literature NP470148.RAeitRrAFY6KiCnY5gsb6wXInB4cDlHMFtdsIB61DK9vA130_provenance.
- NP470148.RAeitRrAFY6KiCnY5gsb6wXInB4cDlHMFtdsIB61DK9vA130_assertion SIO_000772 20685751 NP470148.RAeitRrAFY6KiCnY5gsb6wXInB4cDlHMFtdsIB61DK9vA130_provenance.
- NP470148.RAeitRrAFY6KiCnY5gsb6wXInB4cDlHMFtdsIB61DK9vA130_assertion wasDerivedFrom befree-20140225 NP470148.RAeitRrAFY6KiCnY5gsb6wXInB4cDlHMFtdsIB61DK9vA130_provenance.
- NP470148.RAeitRrAFY6KiCnY5gsb6wXInB4cDlHMFtdsIB61DK9vA130_assertion wasGeneratedBy ECO_0000203 NP470148.RAeitRrAFY6KiCnY5gsb6wXInB4cDlHMFtdsIB61DK9vA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP470148.RAeitRrAFY6KiCnY5gsb6wXInB4cDlHMFtdsIB61DK9vA130_provenance.