Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP483842.RA6HlGYkaGRwIA1A9TVARhCZ6-B6Os-KRTsMVSafludlg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP483842.RA6HlGYkaGRwIA1A9TVARhCZ6-B6Os-KRTsMVSafludlg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP483842.RA6HlGYkaGRwIA1A9TVARhCZ6-B6Os-KRTsMVSafludlg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP483842.RA6HlGYkaGRwIA1A9TVARhCZ6-B6Os-KRTsMVSafludlg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP483842.RA6HlGYkaGRwIA1A9TVARhCZ6-B6Os-KRTsMVSafludlg130_provenance.
- NP483842.RA6HlGYkaGRwIA1A9TVARhCZ6-B6Os-KRTsMVSafludlg130_assertion wasGeneratedBy ECO_0000203 NP483842.RA6HlGYkaGRwIA1A9TVARhCZ6-B6Os-KRTsMVSafludlg130_provenance.
- NP483842.RA6HlGYkaGRwIA1A9TVARhCZ6-B6Os-KRTsMVSafludlg130_assertion wasDerivedFrom befree-20150227 NP483842.RA6HlGYkaGRwIA1A9TVARhCZ6-B6Os-KRTsMVSafludlg130_provenance.
- NP483842.RA6HlGYkaGRwIA1A9TVARhCZ6-B6Os-KRTsMVSafludlg130_assertion SIO_000772 16615080 NP483842.RA6HlGYkaGRwIA1A9TVARhCZ6-B6Os-KRTsMVSafludlg130_provenance.
- NP483842.RA6HlGYkaGRwIA1A9TVARhCZ6-B6Os-KRTsMVSafludlg130_assertion evidence source_evidence_literature NP483842.RA6HlGYkaGRwIA1A9TVARhCZ6-B6Os-KRTsMVSafludlg130_provenance.
- NP483842.RA6HlGYkaGRwIA1A9TVARhCZ6-B6Os-KRTsMVSafludlg130_assertion description "[Novel studies establish that imprinting at one of these, the IGF2-H19 domain, is epigenetically deregulated (with loss of DNA methylation) in Silver-Russell Syndrome (SRS), a congenital disease of growth retardation and asymmetry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP483842.RA6HlGYkaGRwIA1A9TVARhCZ6-B6Os-KRTsMVSafludlg130_provenance.