Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP191274.RADMlwHD_s3xMBlxTDw5HtRPKf4HYacGYqg0OcHJp_UPM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP191274.RADMlwHD_s3xMBlxTDw5HtRPKf4HYacGYqg0OcHJp_UPM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP191274.RADMlwHD_s3xMBlxTDw5HtRPKf4HYacGYqg0OcHJp_UPM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP191274.RADMlwHD_s3xMBlxTDw5HtRPKf4HYacGYqg0OcHJp_UPM130_provenance.
- NP191274.RADMlwHD_s3xMBlxTDw5HtRPKf4HYacGYqg0OcHJp_UPM130_assertion description "[mutational analysis of the entire coding region of DMBT1, employing SSCP analysis and direct DNA sequencing in 79 astrocytic gliomas/somatic mutations were detected.21 of the 27 SNP identified in this study have not been recognized previously.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP191274.RADMlwHD_s3xMBlxTDw5HtRPKf4HYacGYqg0OcHJp_UPM130_provenance.
- NP191274.RADMlwHD_s3xMBlxTDw5HtRPKf4HYacGYqg0OcHJp_UPM130_assertion evidence source_evidence_literature NP191274.RADMlwHD_s3xMBlxTDw5HtRPKf4HYacGYqg0OcHJp_UPM130_provenance.
- NP191274.RADMlwHD_s3xMBlxTDw5HtRPKf4HYacGYqg0OcHJp_UPM130_assertion SIO_000772 12185598 NP191274.RADMlwHD_s3xMBlxTDw5HtRPKf4HYacGYqg0OcHJp_UPM130_provenance.
- NP191274.RADMlwHD_s3xMBlxTDw5HtRPKf4HYacGYqg0OcHJp_UPM130_assertion wasDerivedFrom lhgdn-20090331 NP191274.RADMlwHD_s3xMBlxTDw5HtRPKf4HYacGYqg0OcHJp_UPM130_provenance.
- NP191274.RADMlwHD_s3xMBlxTDw5HtRPKf4HYacGYqg0OcHJp_UPM130_assertion wasGeneratedBy ECO_0000203 NP191274.RADMlwHD_s3xMBlxTDw5HtRPKf4HYacGYqg0OcHJp_UPM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP191274.RADMlwHD_s3xMBlxTDw5HtRPKf4HYacGYqg0OcHJp_UPM130_provenance.