Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1371763.RA83KHNlV1O3VdeXbQOOMNiW8xCauK6FxGDpmvUJG5yi0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1371763.RA83KHNlV1O3VdeXbQOOMNiW8xCauK6FxGDpmvUJG5yi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1371763.RA83KHNlV1O3VdeXbQOOMNiW8xCauK6FxGDpmvUJG5yi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1371763.RA83KHNlV1O3VdeXbQOOMNiW8xCauK6FxGDpmvUJG5yi0130_provenance.
- NP1371763.RA83KHNlV1O3VdeXbQOOMNiW8xCauK6FxGDpmvUJG5yi0130_assertion description "[Fluorescence in situ hybridization (FISH) using cosmid probes for SNRPN, D15S10, and GABRB3 for the Prader-Willi syndrome (PWS)/Angelman syndrome (AS) critical region were not present on the derived chromosome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1371763.RA83KHNlV1O3VdeXbQOOMNiW8xCauK6FxGDpmvUJG5yi0130_provenance.
- NP1371763.RA83KHNlV1O3VdeXbQOOMNiW8xCauK6FxGDpmvUJG5yi0130_assertion evidence source_evidence_literature NP1371763.RA83KHNlV1O3VdeXbQOOMNiW8xCauK6FxGDpmvUJG5yi0130_provenance.
- NP1371763.RA83KHNlV1O3VdeXbQOOMNiW8xCauK6FxGDpmvUJG5yi0130_assertion SIO_000772 9128934 NP1371763.RA83KHNlV1O3VdeXbQOOMNiW8xCauK6FxGDpmvUJG5yi0130_provenance.
- NP1371763.RA83KHNlV1O3VdeXbQOOMNiW8xCauK6FxGDpmvUJG5yi0130_assertion wasDerivedFrom befree-2016 NP1371763.RA83KHNlV1O3VdeXbQOOMNiW8xCauK6FxGDpmvUJG5yi0130_provenance.
- NP1371763.RA83KHNlV1O3VdeXbQOOMNiW8xCauK6FxGDpmvUJG5yi0130_assertion wasGeneratedBy ECO_0000203 NP1371763.RA83KHNlV1O3VdeXbQOOMNiW8xCauK6FxGDpmvUJG5yi0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1371763.RA83KHNlV1O3VdeXbQOOMNiW8xCauK6FxGDpmvUJG5yi0130_provenance.