Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP584723.RA7l1FCbeH2SS3aFCdl8lrzzFy5EpVg1s59T1SJrylLhk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP584723.RA7l1FCbeH2SS3aFCdl8lrzzFy5EpVg1s59T1SJrylLhk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584723.RA7l1FCbeH2SS3aFCdl8lrzzFy5EpVg1s59T1SJrylLhk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584723.RA7l1FCbeH2SS3aFCdl8lrzzFy5EpVg1s59T1SJrylLhk130_provenance.
- NP584723.RA7l1FCbeH2SS3aFCdl8lrzzFy5EpVg1s59T1SJrylLhk130_assertion description "[Combining GISTIC ranking with functional analyses and degree of loss/gain we identify three genes in regions of significant loss (ATP8B1, NARS, and ATP5A1) and eight in regions of gain (CTCFL, SPO11, ZNF217, PLEKHA8, HOXA3, GPNMB, IGF2BP3 and PCAT1) as novel in their association with CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584723.RA7l1FCbeH2SS3aFCdl8lrzzFy5EpVg1s59T1SJrylLhk130_provenance.
- NP584723.RA7l1FCbeH2SS3aFCdl8lrzzFy5EpVg1s59T1SJrylLhk130_assertion evidence source_evidence_literature NP584723.RA7l1FCbeH2SS3aFCdl8lrzzFy5EpVg1s59T1SJrylLhk130_provenance.
- NP584723.RA7l1FCbeH2SS3aFCdl8lrzzFy5EpVg1s59T1SJrylLhk130_assertion SIO_000772 24204606 NP584723.RA7l1FCbeH2SS3aFCdl8lrzzFy5EpVg1s59T1SJrylLhk130_provenance.
- NP584723.RA7l1FCbeH2SS3aFCdl8lrzzFy5EpVg1s59T1SJrylLhk130_assertion wasDerivedFrom befree-20150227 NP584723.RA7l1FCbeH2SS3aFCdl8lrzzFy5EpVg1s59T1SJrylLhk130_provenance.
- NP584723.RA7l1FCbeH2SS3aFCdl8lrzzFy5EpVg1s59T1SJrylLhk130_assertion wasGeneratedBy ECO_0000203 NP584723.RA7l1FCbeH2SS3aFCdl8lrzzFy5EpVg1s59T1SJrylLhk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP584723.RA7l1FCbeH2SS3aFCdl8lrzzFy5EpVg1s59T1SJrylLhk130_provenance.