Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP381351.RAvta9iUpq_4IFg3Rh0bDLIwDAi8bHE8xWBQVMj7GjPpI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP381351.RAvta9iUpq_4IFg3Rh0bDLIwDAi8bHE8xWBQVMj7GjPpI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381351.RAvta9iUpq_4IFg3Rh0bDLIwDAi8bHE8xWBQVMj7GjPpI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381351.RAvta9iUpq_4IFg3Rh0bDLIwDAi8bHE8xWBQVMj7GjPpI130_provenance.
- NP381351.RAvta9iUpq_4IFg3Rh0bDLIwDAi8bHE8xWBQVMj7GjPpI130_assertion description "[Association of single-nucleotide polymorphisms in ERCC1 and ERCC2 with glioma risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381351.RAvta9iUpq_4IFg3Rh0bDLIwDAi8bHE8xWBQVMj7GjPpI130_provenance.
- NP381351.RAvta9iUpq_4IFg3Rh0bDLIwDAi8bHE8xWBQVMj7GjPpI130_assertion evidence source_evidence_literature NP381351.RAvta9iUpq_4IFg3Rh0bDLIwDAi8bHE8xWBQVMj7GjPpI130_provenance.
- NP381351.RAvta9iUpq_4IFg3Rh0bDLIwDAi8bHE8xWBQVMj7GjPpI130_assertion SIO_000772 24782032 NP381351.RAvta9iUpq_4IFg3Rh0bDLIwDAi8bHE8xWBQVMj7GjPpI130_provenance.
- NP381351.RAvta9iUpq_4IFg3Rh0bDLIwDAi8bHE8xWBQVMj7GjPpI130_assertion wasDerivedFrom befree-20150227 NP381351.RAvta9iUpq_4IFg3Rh0bDLIwDAi8bHE8xWBQVMj7GjPpI130_provenance.
- NP381351.RAvta9iUpq_4IFg3Rh0bDLIwDAi8bHE8xWBQVMj7GjPpI130_assertion wasGeneratedBy ECO_0000203 NP381351.RAvta9iUpq_4IFg3Rh0bDLIwDAi8bHE8xWBQVMj7GjPpI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP381351.RAvta9iUpq_4IFg3Rh0bDLIwDAi8bHE8xWBQVMj7GjPpI130_provenance.