Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1380013.RAfi3ocN3Gau8j9O8r3o425KPFi8KlYDiIl1Fodxe3Kw8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1380013.RAfi3ocN3Gau8j9O8r3o425KPFi8KlYDiIl1Fodxe3Kw8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1380013.RAfi3ocN3Gau8j9O8r3o425KPFi8KlYDiIl1Fodxe3Kw8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1380013.RAfi3ocN3Gau8j9O8r3o425KPFi8KlYDiIl1Fodxe3Kw8130_provenance.
- NP1380013.RAfi3ocN3Gau8j9O8r3o425KPFi8KlYDiIl1Fodxe3Kw8130_assertion description "[The major phenotypic features of AS correlate with the loss of maternal-specific expression of Ube3a in hippocampus and cerebellum as revealed in the mouse model.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1380013.RAfi3ocN3Gau8j9O8r3o425KPFi8KlYDiIl1Fodxe3Kw8130_provenance.
- NP1380013.RAfi3ocN3Gau8j9O8r3o425KPFi8KlYDiIl1Fodxe3Kw8130_assertion evidence source_evidence_literature NP1380013.RAfi3ocN3Gau8j9O8r3o425KPFi8KlYDiIl1Fodxe3Kw8130_provenance.
- NP1380013.RAfi3ocN3Gau8j9O8r3o425KPFi8KlYDiIl1Fodxe3Kw8130_assertion SIO_000772 9288101 NP1380013.RAfi3ocN3Gau8j9O8r3o425KPFi8KlYDiIl1Fodxe3Kw8130_provenance.
- NP1380013.RAfi3ocN3Gau8j9O8r3o425KPFi8KlYDiIl1Fodxe3Kw8130_assertion wasDerivedFrom befree-2016 NP1380013.RAfi3ocN3Gau8j9O8r3o425KPFi8KlYDiIl1Fodxe3Kw8130_provenance.
- NP1380013.RAfi3ocN3Gau8j9O8r3o425KPFi8KlYDiIl1Fodxe3Kw8130_assertion wasGeneratedBy ECO_0000203 NP1380013.RAfi3ocN3Gau8j9O8r3o425KPFi8KlYDiIl1Fodxe3Kw8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1380013.RAfi3ocN3Gau8j9O8r3o425KPFi8KlYDiIl1Fodxe3Kw8130_provenance.