Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_provenance.
- NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_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." NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_provenance.
- NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_assertion evidence source_evidence_literature NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_provenance.
- NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_assertion SIO_000772 20876107 NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_provenance.
- NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_assertion wasDerivedFrom befree-20150227 NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_provenance.
- NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_assertion wasGeneratedBy ECO_0000203 NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP764983.RANv0MVyBR86B57ejGfBWZ60D_dRvyKCQJ4HcapbF36Lc130_provenance.