Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP862848.RA8ptiz7gFP8ZTIxmtEsEnQmDkpkmvoJl1p4DwJVQ4wqc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP862848.RA8ptiz7gFP8ZTIxmtEsEnQmDkpkmvoJl1p4DwJVQ4wqc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP862848.RA8ptiz7gFP8ZTIxmtEsEnQmDkpkmvoJl1p4DwJVQ4wqc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP862848.RA8ptiz7gFP8ZTIxmtEsEnQmDkpkmvoJl1p4DwJVQ4wqc130_provenance.
- NP862848.RA8ptiz7gFP8ZTIxmtEsEnQmDkpkmvoJl1p4DwJVQ4wqc130_assertion description "[Angelman syndrome (AS) is a neurodevelopmental disorder caused by a lack of expression of the maternal copy of UBE3A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862848.RA8ptiz7gFP8ZTIxmtEsEnQmDkpkmvoJl1p4DwJVQ4wqc130_provenance.
- NP862848.RA8ptiz7gFP8ZTIxmtEsEnQmDkpkmvoJl1p4DwJVQ4wqc130_assertion evidence source_evidence_literature NP862848.RA8ptiz7gFP8ZTIxmtEsEnQmDkpkmvoJl1p4DwJVQ4wqc130_provenance.
- NP862848.RA8ptiz7gFP8ZTIxmtEsEnQmDkpkmvoJl1p4DwJVQ4wqc130_assertion SIO_000772 21204213 NP862848.RA8ptiz7gFP8ZTIxmtEsEnQmDkpkmvoJl1p4DwJVQ4wqc130_provenance.
- NP862848.RA8ptiz7gFP8ZTIxmtEsEnQmDkpkmvoJl1p4DwJVQ4wqc130_assertion wasDerivedFrom befree-2016 NP862848.RA8ptiz7gFP8ZTIxmtEsEnQmDkpkmvoJl1p4DwJVQ4wqc130_provenance.
- NP862848.RA8ptiz7gFP8ZTIxmtEsEnQmDkpkmvoJl1p4DwJVQ4wqc130_assertion wasGeneratedBy ECO_0000203 NP862848.RA8ptiz7gFP8ZTIxmtEsEnQmDkpkmvoJl1p4DwJVQ4wqc130_provenance.
- befree-2016 importedOn "2016-02-19" NP862848.RA8ptiz7gFP8ZTIxmtEsEnQmDkpkmvoJl1p4DwJVQ4wqc130_provenance.