Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP279125.RA5paGKe8Qt7qIkjjq7No0a0Bqq75gwPnSMnOU3iYbSMc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP279125.RA5paGKe8Qt7qIkjjq7No0a0Bqq75gwPnSMnOU3iYbSMc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP279125.RA5paGKe8Qt7qIkjjq7No0a0Bqq75gwPnSMnOU3iYbSMc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP279125.RA5paGKe8Qt7qIkjjq7No0a0Bqq75gwPnSMnOU3iYbSMc130_provenance.
- NP279125.RA5paGKe8Qt7qIkjjq7No0a0Bqq75gwPnSMnOU3iYbSMc130_assertion description "[Despite the high frequency of LOH at 1p32 microsatellite markers, the lack of genetic and epigenetic aberrations in the p18 gene together with the presence of p18 protein in all but one meningioma samples argues against the role of p18 as a tumour suppressor gene important for meningioma development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279125.RA5paGKe8Qt7qIkjjq7No0a0Bqq75gwPnSMnOU3iYbSMc130_provenance.
- NP279125.RA5paGKe8Qt7qIkjjq7No0a0Bqq75gwPnSMnOU3iYbSMc130_assertion evidence source_evidence_literature NP279125.RA5paGKe8Qt7qIkjjq7No0a0Bqq75gwPnSMnOU3iYbSMc130_provenance.
- NP279125.RA5paGKe8Qt7qIkjjq7No0a0Bqq75gwPnSMnOU3iYbSMc130_assertion SIO_000772 10736068 NP279125.RA5paGKe8Qt7qIkjjq7No0a0Bqq75gwPnSMnOU3iYbSMc130_provenance.
- NP279125.RA5paGKe8Qt7qIkjjq7No0a0Bqq75gwPnSMnOU3iYbSMc130_assertion wasDerivedFrom befree-2016 NP279125.RA5paGKe8Qt7qIkjjq7No0a0Bqq75gwPnSMnOU3iYbSMc130_provenance.
- NP279125.RA5paGKe8Qt7qIkjjq7No0a0Bqq75gwPnSMnOU3iYbSMc130_assertion wasGeneratedBy ECO_0000203 NP279125.RA5paGKe8Qt7qIkjjq7No0a0Bqq75gwPnSMnOU3iYbSMc130_provenance.
- befree-2016 importedOn "2016-02-19" NP279125.RA5paGKe8Qt7qIkjjq7No0a0Bqq75gwPnSMnOU3iYbSMc130_provenance.