Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP587519.RAnCRHWmNVIcSXn4KeAgl2B2uNhrlokUxE4h83-dfpC58130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP587519.RAnCRHWmNVIcSXn4KeAgl2B2uNhrlokUxE4h83-dfpC58130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP587519.RAnCRHWmNVIcSXn4KeAgl2B2uNhrlokUxE4h83-dfpC58130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP587519.RAnCRHWmNVIcSXn4KeAgl2B2uNhrlokUxE4h83-dfpC58130_provenance.
- NP587519.RAnCRHWmNVIcSXn4KeAgl2B2uNhrlokUxE4h83-dfpC58130_assertion description "[Array-based comparative genomic hybridization demonstrated partial trisomy 7p (7p15.3-p22.3) and partial monosomy 13q (13q33.3-q34).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587519.RAnCRHWmNVIcSXn4KeAgl2B2uNhrlokUxE4h83-dfpC58130_provenance.
- NP587519.RAnCRHWmNVIcSXn4KeAgl2B2uNhrlokUxE4h83-dfpC58130_assertion evidence source_evidence_literature NP587519.RAnCRHWmNVIcSXn4KeAgl2B2uNhrlokUxE4h83-dfpC58130_provenance.
- NP587519.RAnCRHWmNVIcSXn4KeAgl2B2uNhrlokUxE4h83-dfpC58130_assertion SIO_000772 21056318 NP587519.RAnCRHWmNVIcSXn4KeAgl2B2uNhrlokUxE4h83-dfpC58130_provenance.
- NP587519.RAnCRHWmNVIcSXn4KeAgl2B2uNhrlokUxE4h83-dfpC58130_assertion wasDerivedFrom befree-20140225 NP587519.RAnCRHWmNVIcSXn4KeAgl2B2uNhrlokUxE4h83-dfpC58130_provenance.
- NP587519.RAnCRHWmNVIcSXn4KeAgl2B2uNhrlokUxE4h83-dfpC58130_assertion wasGeneratedBy ECO_0000203 NP587519.RAnCRHWmNVIcSXn4KeAgl2B2uNhrlokUxE4h83-dfpC58130_provenance.
- befree-20140225 importedOn "2014-02-25" NP587519.RAnCRHWmNVIcSXn4KeAgl2B2uNhrlokUxE4h83-dfpC58130_provenance.