Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP908049.RAklugT3_cCJBh5_r763414-11X_o1x56-iGbN-REBERU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP908049.RAklugT3_cCJBh5_r763414-11X_o1x56-iGbN-REBERU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP908049.RAklugT3_cCJBh5_r763414-11X_o1x56-iGbN-REBERU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP908049.RAklugT3_cCJBh5_r763414-11X_o1x56-iGbN-REBERU130_provenance.
- NP908049.RAklugT3_cCJBh5_r763414-11X_o1x56-iGbN-REBERU130_assertion description "[We present two cancer-free dysmorphic patients with karyotypes of 46,XX,del(5)(q15q22.3) and 46,XX,del(3)(p25.2~pter).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908049.RAklugT3_cCJBh5_r763414-11X_o1x56-iGbN-REBERU130_provenance.
- NP908049.RAklugT3_cCJBh5_r763414-11X_o1x56-iGbN-REBERU130_assertion evidence source_evidence_literature NP908049.RAklugT3_cCJBh5_r763414-11X_o1x56-iGbN-REBERU130_provenance.
- NP908049.RAklugT3_cCJBh5_r763414-11X_o1x56-iGbN-REBERU130_assertion SIO_000772 17954272 NP908049.RAklugT3_cCJBh5_r763414-11X_o1x56-iGbN-REBERU130_provenance.
- NP908049.RAklugT3_cCJBh5_r763414-11X_o1x56-iGbN-REBERU130_assertion wasDerivedFrom befree-20140225 NP908049.RAklugT3_cCJBh5_r763414-11X_o1x56-iGbN-REBERU130_provenance.
- NP908049.RAklugT3_cCJBh5_r763414-11X_o1x56-iGbN-REBERU130_assertion wasGeneratedBy ECO_0000203 NP908049.RAklugT3_cCJBh5_r763414-11X_o1x56-iGbN-REBERU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP908049.RAklugT3_cCJBh5_r763414-11X_o1x56-iGbN-REBERU130_provenance.