Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP316915.RAmlCA7tujWs1WfnZ8L39QZnjvP2PJvx1TNnWOo82GVsA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP316915.RAmlCA7tujWs1WfnZ8L39QZnjvP2PJvx1TNnWOo82GVsA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316915.RAmlCA7tujWs1WfnZ8L39QZnjvP2PJvx1TNnWOo82GVsA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316915.RAmlCA7tujWs1WfnZ8L39QZnjvP2PJvx1TNnWOo82GVsA130_provenance.
- NP316915.RAmlCA7tujWs1WfnZ8L39QZnjvP2PJvx1TNnWOo82GVsA130_assertion description "[Our data suggest that lineage-specific methylation-associated gene silencing of survivin, CHK2, and WT1 in MDS hematopoietic precursor cells may contribute to the MDS-specific phenotype]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316915.RAmlCA7tujWs1WfnZ8L39QZnjvP2PJvx1TNnWOo82GVsA130_provenance.
- NP316915.RAmlCA7tujWs1WfnZ8L39QZnjvP2PJvx1TNnWOo82GVsA130_assertion evidence source_evidence_literature NP316915.RAmlCA7tujWs1WfnZ8L39QZnjvP2PJvx1TNnWOo82GVsA130_provenance.
- NP316915.RAmlCA7tujWs1WfnZ8L39QZnjvP2PJvx1TNnWOo82GVsA130_assertion SIO_000772 17577921 NP316915.RAmlCA7tujWs1WfnZ8L39QZnjvP2PJvx1TNnWOo82GVsA130_provenance.
- NP316915.RAmlCA7tujWs1WfnZ8L39QZnjvP2PJvx1TNnWOo82GVsA130_assertion wasDerivedFrom befree-20140225 NP316915.RAmlCA7tujWs1WfnZ8L39QZnjvP2PJvx1TNnWOo82GVsA130_provenance.
- NP316915.RAmlCA7tujWs1WfnZ8L39QZnjvP2PJvx1TNnWOo82GVsA130_assertion wasGeneratedBy ECO_0000203 NP316915.RAmlCA7tujWs1WfnZ8L39QZnjvP2PJvx1TNnWOo82GVsA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP316915.RAmlCA7tujWs1WfnZ8L39QZnjvP2PJvx1TNnWOo82GVsA130_provenance.