Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP788886.RAZIO5a8AWOsPa9T6jY56sNoeXSsfP5Dky9uBuWwYZOkU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP788886.RAZIO5a8AWOsPa9T6jY56sNoeXSsfP5Dky9uBuWwYZOkU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788886.RAZIO5a8AWOsPa9T6jY56sNoeXSsfP5Dky9uBuWwYZOkU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788886.RAZIO5a8AWOsPa9T6jY56sNoeXSsfP5Dky9uBuWwYZOkU130_provenance.
- NP788886.RAZIO5a8AWOsPa9T6jY56sNoeXSsfP5Dky9uBuWwYZOkU130_assertion description "[Besides, there is no report about the association between NBS1 3'UTR variant rs2735383 and ALL risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788886.RAZIO5a8AWOsPa9T6jY56sNoeXSsfP5Dky9uBuWwYZOkU130_provenance.
- NP788886.RAZIO5a8AWOsPa9T6jY56sNoeXSsfP5Dky9uBuWwYZOkU130_assertion evidence source_evidence_literature NP788886.RAZIO5a8AWOsPa9T6jY56sNoeXSsfP5Dky9uBuWwYZOkU130_provenance.
- NP788886.RAZIO5a8AWOsPa9T6jY56sNoeXSsfP5Dky9uBuWwYZOkU130_assertion SIO_000772 21166880 NP788886.RAZIO5a8AWOsPa9T6jY56sNoeXSsfP5Dky9uBuWwYZOkU130_provenance.
- NP788886.RAZIO5a8AWOsPa9T6jY56sNoeXSsfP5Dky9uBuWwYZOkU130_assertion wasDerivedFrom befree-20140225 NP788886.RAZIO5a8AWOsPa9T6jY56sNoeXSsfP5Dky9uBuWwYZOkU130_provenance.
- NP788886.RAZIO5a8AWOsPa9T6jY56sNoeXSsfP5Dky9uBuWwYZOkU130_assertion wasGeneratedBy ECO_0000203 NP788886.RAZIO5a8AWOsPa9T6jY56sNoeXSsfP5Dky9uBuWwYZOkU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP788886.RAZIO5a8AWOsPa9T6jY56sNoeXSsfP5Dky9uBuWwYZOkU130_provenance.