Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP366547.RAI1yRdnH5TTSYSHTL8q-GSAdT6vSuzMLl6IUd9vySrUQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP366547.RAI1yRdnH5TTSYSHTL8q-GSAdT6vSuzMLl6IUd9vySrUQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP366547.RAI1yRdnH5TTSYSHTL8q-GSAdT6vSuzMLl6IUd9vySrUQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP366547.RAI1yRdnH5TTSYSHTL8q-GSAdT6vSuzMLl6IUd9vySrUQ130_provenance.
- NP366547.RAI1yRdnH5TTSYSHTL8q-GSAdT6vSuzMLl6IUd9vySrUQ130_assertion description "[In addition, FISH, with probes at D15S11 and GABR beta 3 from the Prader-Willi syndrome/Angelman's syndrome region, was performed on a subset of 25 of these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP366547.RAI1yRdnH5TTSYSHTL8q-GSAdT6vSuzMLl6IUd9vySrUQ130_provenance.
- NP366547.RAI1yRdnH5TTSYSHTL8q-GSAdT6vSuzMLl6IUd9vySrUQ130_assertion evidence source_evidence_literature NP366547.RAI1yRdnH5TTSYSHTL8q-GSAdT6vSuzMLl6IUd9vySrUQ130_provenance.
- NP366547.RAI1yRdnH5TTSYSHTL8q-GSAdT6vSuzMLl6IUd9vySrUQ130_assertion SIO_000772 7618904 NP366547.RAI1yRdnH5TTSYSHTL8q-GSAdT6vSuzMLl6IUd9vySrUQ130_provenance.
- NP366547.RAI1yRdnH5TTSYSHTL8q-GSAdT6vSuzMLl6IUd9vySrUQ130_assertion wasDerivedFrom befree-20150227 NP366547.RAI1yRdnH5TTSYSHTL8q-GSAdT6vSuzMLl6IUd9vySrUQ130_provenance.
- NP366547.RAI1yRdnH5TTSYSHTL8q-GSAdT6vSuzMLl6IUd9vySrUQ130_assertion wasGeneratedBy ECO_0000203 NP366547.RAI1yRdnH5TTSYSHTL8q-GSAdT6vSuzMLl6IUd9vySrUQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP366547.RAI1yRdnH5TTSYSHTL8q-GSAdT6vSuzMLl6IUd9vySrUQ130_provenance.