Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP842147.RA8wQbemVvMJ7ISCBedCKI3TPqAB8_Z_bg0oGXyH7Q6gw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP842147.RA8wQbemVvMJ7ISCBedCKI3TPqAB8_Z_bg0oGXyH7Q6gw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP842147.RA8wQbemVvMJ7ISCBedCKI3TPqAB8_Z_bg0oGXyH7Q6gw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP842147.RA8wQbemVvMJ7ISCBedCKI3TPqAB8_Z_bg0oGXyH7Q6gw130_provenance.
- NP842147.RA8wQbemVvMJ7ISCBedCKI3TPqAB8_Z_bg0oGXyH7Q6gw130_assertion description "[These iPSC models of genomic imprinting disorders will facilitate investigation of the AS and PWS disease processes and allow study of the developmental timing and mechanism of UBE3A repression in human neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP842147.RA8wQbemVvMJ7ISCBedCKI3TPqAB8_Z_bg0oGXyH7Q6gw130_provenance.
- NP842147.RA8wQbemVvMJ7ISCBedCKI3TPqAB8_Z_bg0oGXyH7Q6gw130_assertion evidence source_evidence_literature NP842147.RA8wQbemVvMJ7ISCBedCKI3TPqAB8_Z_bg0oGXyH7Q6gw130_provenance.
- NP842147.RA8wQbemVvMJ7ISCBedCKI3TPqAB8_Z_bg0oGXyH7Q6gw130_assertion SIO_000772 20876107 NP842147.RA8wQbemVvMJ7ISCBedCKI3TPqAB8_Z_bg0oGXyH7Q6gw130_provenance.
- NP842147.RA8wQbemVvMJ7ISCBedCKI3TPqAB8_Z_bg0oGXyH7Q6gw130_assertion wasDerivedFrom befree-2016 NP842147.RA8wQbemVvMJ7ISCBedCKI3TPqAB8_Z_bg0oGXyH7Q6gw130_provenance.
- NP842147.RA8wQbemVvMJ7ISCBedCKI3TPqAB8_Z_bg0oGXyH7Q6gw130_assertion wasGeneratedBy ECO_0000203 NP842147.RA8wQbemVvMJ7ISCBedCKI3TPqAB8_Z_bg0oGXyH7Q6gw130_provenance.
- befree-2016 importedOn "2016-02-19" NP842147.RA8wQbemVvMJ7ISCBedCKI3TPqAB8_Z_bg0oGXyH7Q6gw130_provenance.