Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP648821.RAkOKfOTBXLvRT3mI9l723Ex_MsjMYuneUPUc7D8i6oY0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP648821.RAkOKfOTBXLvRT3mI9l723Ex_MsjMYuneUPUc7D8i6oY0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP648821.RAkOKfOTBXLvRT3mI9l723Ex_MsjMYuneUPUc7D8i6oY0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP648821.RAkOKfOTBXLvRT3mI9l723Ex_MsjMYuneUPUc7D8i6oY0130_provenance.
- NP648821.RAkOKfOTBXLvRT3mI9l723Ex_MsjMYuneUPUc7D8i6oY0130_assertion description "[Using an integrated approach for genome-wide methylation and copy number analyses, we identified SLC5A8 on chromosome 12q23.1 that was affected frequently by aberrant methylation in human astrocytomas and oligodendrogliomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648821.RAkOKfOTBXLvRT3mI9l723Ex_MsjMYuneUPUc7D8i6oY0130_provenance.
- NP648821.RAkOKfOTBXLvRT3mI9l723Ex_MsjMYuneUPUc7D8i6oY0130_assertion evidence source_evidence_literature NP648821.RAkOKfOTBXLvRT3mI9l723Ex_MsjMYuneUPUc7D8i6oY0130_provenance.
- NP648821.RAkOKfOTBXLvRT3mI9l723Ex_MsjMYuneUPUc7D8i6oY0130_assertion SIO_000772 15867356 NP648821.RAkOKfOTBXLvRT3mI9l723Ex_MsjMYuneUPUc7D8i6oY0130_provenance.
- NP648821.RAkOKfOTBXLvRT3mI9l723Ex_MsjMYuneUPUc7D8i6oY0130_assertion wasDerivedFrom befree-20140225 NP648821.RAkOKfOTBXLvRT3mI9l723Ex_MsjMYuneUPUc7D8i6oY0130_provenance.
- NP648821.RAkOKfOTBXLvRT3mI9l723Ex_MsjMYuneUPUc7D8i6oY0130_assertion wasGeneratedBy ECO_0000203 NP648821.RAkOKfOTBXLvRT3mI9l723Ex_MsjMYuneUPUc7D8i6oY0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP648821.RAkOKfOTBXLvRT3mI9l723Ex_MsjMYuneUPUc7D8i6oY0130_provenance.