Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP737006.RA0bg7k1DlACJFfyoY6Y9PXYHEDA36T1HeCRvwiqg_enM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP737006.RA0bg7k1DlACJFfyoY6Y9PXYHEDA36T1HeCRvwiqg_enM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP737006.RA0bg7k1DlACJFfyoY6Y9PXYHEDA36T1HeCRvwiqg_enM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP737006.RA0bg7k1DlACJFfyoY6Y9PXYHEDA36T1HeCRvwiqg_enM130_provenance.
- NP737006.RA0bg7k1DlACJFfyoY6Y9PXYHEDA36T1HeCRvwiqg_enM130_assertion description "[An infant with multiple anomalies and developmental delay during his first year was found to have an intersitital deletion of band p14 from the proximal short arm of chromosome 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP737006.RA0bg7k1DlACJFfyoY6Y9PXYHEDA36T1HeCRvwiqg_enM130_provenance.
- NP737006.RA0bg7k1DlACJFfyoY6Y9PXYHEDA36T1HeCRvwiqg_enM130_assertion evidence source_evidence_literature NP737006.RA0bg7k1DlACJFfyoY6Y9PXYHEDA36T1HeCRvwiqg_enM130_provenance.
- NP737006.RA0bg7k1DlACJFfyoY6Y9PXYHEDA36T1HeCRvwiqg_enM130_assertion SIO_000772 7424912 NP737006.RA0bg7k1DlACJFfyoY6Y9PXYHEDA36T1HeCRvwiqg_enM130_provenance.
- NP737006.RA0bg7k1DlACJFfyoY6Y9PXYHEDA36T1HeCRvwiqg_enM130_assertion wasDerivedFrom befree-20140225 NP737006.RA0bg7k1DlACJFfyoY6Y9PXYHEDA36T1HeCRvwiqg_enM130_provenance.
- NP737006.RA0bg7k1DlACJFfyoY6Y9PXYHEDA36T1HeCRvwiqg_enM130_assertion wasGeneratedBy ECO_0000203 NP737006.RA0bg7k1DlACJFfyoY6Y9PXYHEDA36T1HeCRvwiqg_enM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP737006.RA0bg7k1DlACJFfyoY6Y9PXYHEDA36T1HeCRvwiqg_enM130_provenance.