Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP558329.RALx1KX3MVuzcAxbsvWR0WFNqspPbBHuhGt4dEYCcDaJg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP558329.RALx1KX3MVuzcAxbsvWR0WFNqspPbBHuhGt4dEYCcDaJg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP558329.RALx1KX3MVuzcAxbsvWR0WFNqspPbBHuhGt4dEYCcDaJg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP558329.RALx1KX3MVuzcAxbsvWR0WFNqspPbBHuhGt4dEYCcDaJg130_provenance.
- NP558329.RALx1KX3MVuzcAxbsvWR0WFNqspPbBHuhGt4dEYCcDaJg130_assertion description "[We identified frequent methylation of RASSF1 and MGMT and infrequent methylation of MLH1 and DAPK1 in cases of concomitant TCC and SCBC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP558329.RALx1KX3MVuzcAxbsvWR0WFNqspPbBHuhGt4dEYCcDaJg130_provenance.
- NP558329.RALx1KX3MVuzcAxbsvWR0WFNqspPbBHuhGt4dEYCcDaJg130_assertion evidence source_evidence_literature NP558329.RALx1KX3MVuzcAxbsvWR0WFNqspPbBHuhGt4dEYCcDaJg130_provenance.
- NP558329.RALx1KX3MVuzcAxbsvWR0WFNqspPbBHuhGt4dEYCcDaJg130_assertion SIO_000772 18192966 NP558329.RALx1KX3MVuzcAxbsvWR0WFNqspPbBHuhGt4dEYCcDaJg130_provenance.
- NP558329.RALx1KX3MVuzcAxbsvWR0WFNqspPbBHuhGt4dEYCcDaJg130_assertion wasDerivedFrom befree-20140225 NP558329.RALx1KX3MVuzcAxbsvWR0WFNqspPbBHuhGt4dEYCcDaJg130_provenance.
- NP558329.RALx1KX3MVuzcAxbsvWR0WFNqspPbBHuhGt4dEYCcDaJg130_assertion wasGeneratedBy ECO_0000203 NP558329.RALx1KX3MVuzcAxbsvWR0WFNqspPbBHuhGt4dEYCcDaJg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP558329.RALx1KX3MVuzcAxbsvWR0WFNqspPbBHuhGt4dEYCcDaJg130_provenance.