Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_provenance.
- NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_assertion description "[Variability in clinical phenotype despite common chromosomal deletion in Smith-Magenis syndrome [del(17)(p11.2p11.2)].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_provenance.
- NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_assertion evidence source_evidence_literature NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_provenance.
- NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_assertion SIO_000772 14614393 NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_provenance.
- NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_assertion wasDerivedFrom befree-20140225 NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_provenance.
- NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_assertion wasGeneratedBy ECO_0000203 NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_provenance.