Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP44911.RAeu5NBXFtXeelJw1M17TVGGDhufA39xxEvRLWS-jEAKQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP44911.RAeu5NBXFtXeelJw1M17TVGGDhufA39xxEvRLWS-jEAKQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP44911.RAeu5NBXFtXeelJw1M17TVGGDhufA39xxEvRLWS-jEAKQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP44911.RAeu5NBXFtXeelJw1M17TVGGDhufA39xxEvRLWS-jEAKQ130_provenance.
- NP44911.RAeu5NBXFtXeelJw1M17TVGGDhufA39xxEvRLWS-jEAKQ130_assertion description "[We genotyped constitutive variants ERCC1 C8092A and ERCC2 K751Q and R156R in approximately 450 adults with glioma and 500 controls from two independent population-based series, uniformly reviewed patients' tumors to determine histopathologic category, and determined a variety of tumor markers among astrocytic tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44911.RAeu5NBXFtXeelJw1M17TVGGDhufA39xxEvRLWS-jEAKQ130_provenance.
- NP44911.RAeu5NBXFtXeelJw1M17TVGGDhufA39xxEvRLWS-jEAKQ130_assertion evidence source_evidence_literature NP44911.RAeu5NBXFtXeelJw1M17TVGGDhufA39xxEvRLWS-jEAKQ130_provenance.
- NP44911.RAeu5NBXFtXeelJw1M17TVGGDhufA39xxEvRLWS-jEAKQ130_assertion SIO_000772 16212814 NP44911.RAeu5NBXFtXeelJw1M17TVGGDhufA39xxEvRLWS-jEAKQ130_provenance.
- NP44911.RAeu5NBXFtXeelJw1M17TVGGDhufA39xxEvRLWS-jEAKQ130_assertion wasDerivedFrom gad-20130706 NP44911.RAeu5NBXFtXeelJw1M17TVGGDhufA39xxEvRLWS-jEAKQ130_provenance.
- NP44911.RAeu5NBXFtXeelJw1M17TVGGDhufA39xxEvRLWS-jEAKQ130_assertion wasGeneratedBy ECO_0000203 NP44911.RAeu5NBXFtXeelJw1M17TVGGDhufA39xxEvRLWS-jEAKQ130_provenance.
- gad-20130706 importedOn "2013-07-06" NP44911.RAeu5NBXFtXeelJw1M17TVGGDhufA39xxEvRLWS-jEAKQ130_provenance.