Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP245814.RANLiqWVtxtHnlIIYaNGikUenzDXmulSYH9fOaT9q7ZxY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP245814.RANLiqWVtxtHnlIIYaNGikUenzDXmulSYH9fOaT9q7ZxY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP245814.RANLiqWVtxtHnlIIYaNGikUenzDXmulSYH9fOaT9q7ZxY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP245814.RANLiqWVtxtHnlIIYaNGikUenzDXmulSYH9fOaT9q7ZxY130_provenance.
- NP245814.RANLiqWVtxtHnlIIYaNGikUenzDXmulSYH9fOaT9q7ZxY130_assertion description "[Loss of heterozygosity (LOH) for p73 was observed in 19% (28/151) of informative cases which included 92 mass-screening (MS) tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP245814.RANLiqWVtxtHnlIIYaNGikUenzDXmulSYH9fOaT9q7ZxY130_provenance.
- NP245814.RANLiqWVtxtHnlIIYaNGikUenzDXmulSYH9fOaT9q7ZxY130_assertion evidence source_evidence_literature NP245814.RANLiqWVtxtHnlIIYaNGikUenzDXmulSYH9fOaT9q7ZxY130_provenance.
- NP245814.RANLiqWVtxtHnlIIYaNGikUenzDXmulSYH9fOaT9q7ZxY130_assertion SIO_000772 10023682 NP245814.RANLiqWVtxtHnlIIYaNGikUenzDXmulSYH9fOaT9q7ZxY130_provenance.
- NP245814.RANLiqWVtxtHnlIIYaNGikUenzDXmulSYH9fOaT9q7ZxY130_assertion wasDerivedFrom befree-2016 NP245814.RANLiqWVtxtHnlIIYaNGikUenzDXmulSYH9fOaT9q7ZxY130_provenance.
- NP245814.RANLiqWVtxtHnlIIYaNGikUenzDXmulSYH9fOaT9q7ZxY130_assertion wasGeneratedBy ECO_0000203 NP245814.RANLiqWVtxtHnlIIYaNGikUenzDXmulSYH9fOaT9q7ZxY130_provenance.
- befree-2016 importedOn "2016-02-19" NP245814.RANLiqWVtxtHnlIIYaNGikUenzDXmulSYH9fOaT9q7ZxY130_provenance.