Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP971425.RAoQU3Ee6gGcLSYQTbV1ftFahGDeHD_AJM3tgasy_iMi0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP971425.RAoQU3Ee6gGcLSYQTbV1ftFahGDeHD_AJM3tgasy_iMi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP971425.RAoQU3Ee6gGcLSYQTbV1ftFahGDeHD_AJM3tgasy_iMi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP971425.RAoQU3Ee6gGcLSYQTbV1ftFahGDeHD_AJM3tgasy_iMi0130_provenance.
- NP971425.RAoQU3Ee6gGcLSYQTbV1ftFahGDeHD_AJM3tgasy_iMi0130_assertion description "[In addition, this study is one of the largest GST polymorphism studies undertaken in the Spanish population and the first time that copy number variants have been scrutinized in relation to MM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP971425.RAoQU3Ee6gGcLSYQTbV1ftFahGDeHD_AJM3tgasy_iMi0130_provenance.
- NP971425.RAoQU3Ee6gGcLSYQTbV1ftFahGDeHD_AJM3tgasy_iMi0130_assertion evidence source_evidence_literature NP971425.RAoQU3Ee6gGcLSYQTbV1ftFahGDeHD_AJM3tgasy_iMi0130_provenance.
- NP971425.RAoQU3Ee6gGcLSYQTbV1ftFahGDeHD_AJM3tgasy_iMi0130_assertion SIO_000772 22251241 NP971425.RAoQU3Ee6gGcLSYQTbV1ftFahGDeHD_AJM3tgasy_iMi0130_provenance.
- NP971425.RAoQU3Ee6gGcLSYQTbV1ftFahGDeHD_AJM3tgasy_iMi0130_assertion wasDerivedFrom befree-20150227 NP971425.RAoQU3Ee6gGcLSYQTbV1ftFahGDeHD_AJM3tgasy_iMi0130_provenance.
- NP971425.RAoQU3Ee6gGcLSYQTbV1ftFahGDeHD_AJM3tgasy_iMi0130_assertion wasGeneratedBy ECO_0000203 NP971425.RAoQU3Ee6gGcLSYQTbV1ftFahGDeHD_AJM3tgasy_iMi0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP971425.RAoQU3Ee6gGcLSYQTbV1ftFahGDeHD_AJM3tgasy_iMi0130_provenance.