Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP193688.RAmXv_7GTpSw0alwI5HawwmJg54NDR2XhXCRSLW3Qg8BU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP193688.RAmXv_7GTpSw0alwI5HawwmJg54NDR2XhXCRSLW3Qg8BU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193688.RAmXv_7GTpSw0alwI5HawwmJg54NDR2XhXCRSLW3Qg8BU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193688.RAmXv_7GTpSw0alwI5HawwmJg54NDR2XhXCRSLW3Qg8BU130_provenance.
- NP193688.RAmXv_7GTpSw0alwI5HawwmJg54NDR2XhXCRSLW3Qg8BU130_assertion description "[This review summarizes recent studies on applications of molecular markers such as chromosome 1p/19q codeletion and MGMT status in the treatment of glioma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193688.RAmXv_7GTpSw0alwI5HawwmJg54NDR2XhXCRSLW3Qg8BU130_provenance.
- NP193688.RAmXv_7GTpSw0alwI5HawwmJg54NDR2XhXCRSLW3Qg8BU130_assertion evidence source_evidence_literature NP193688.RAmXv_7GTpSw0alwI5HawwmJg54NDR2XhXCRSLW3Qg8BU130_provenance.
- NP193688.RAmXv_7GTpSw0alwI5HawwmJg54NDR2XhXCRSLW3Qg8BU130_assertion SIO_000772 17906460 NP193688.RAmXv_7GTpSw0alwI5HawwmJg54NDR2XhXCRSLW3Qg8BU130_provenance.
- NP193688.RAmXv_7GTpSw0alwI5HawwmJg54NDR2XhXCRSLW3Qg8BU130_assertion wasDerivedFrom befree-20140225 NP193688.RAmXv_7GTpSw0alwI5HawwmJg54NDR2XhXCRSLW3Qg8BU130_provenance.
- NP193688.RAmXv_7GTpSw0alwI5HawwmJg54NDR2XhXCRSLW3Qg8BU130_assertion wasGeneratedBy ECO_0000203 NP193688.RAmXv_7GTpSw0alwI5HawwmJg54NDR2XhXCRSLW3Qg8BU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP193688.RAmXv_7GTpSw0alwI5HawwmJg54NDR2XhXCRSLW3Qg8BU130_provenance.