Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP301576.RAyad_MYDbtVchUMZqg1pYhSHz3InoKWPp17ZLdh2hKwY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP301576.RAyad_MYDbtVchUMZqg1pYhSHz3InoKWPp17ZLdh2hKwY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP301576.RAyad_MYDbtVchUMZqg1pYhSHz3InoKWPp17ZLdh2hKwY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP301576.RAyad_MYDbtVchUMZqg1pYhSHz3InoKWPp17ZLdh2hKwY130_provenance.
- NP301576.RAyad_MYDbtVchUMZqg1pYhSHz3InoKWPp17ZLdh2hKwY130_assertion description "[In total, nine astrocytomas (45%) exhibited homozygous P16ink4 deletion or CDK4 gene amplification, but only one PNET (5%) demonstrated either gene alteration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP301576.RAyad_MYDbtVchUMZqg1pYhSHz3InoKWPp17ZLdh2hKwY130_provenance.
- NP301576.RAyad_MYDbtVchUMZqg1pYhSHz3InoKWPp17ZLdh2hKwY130_assertion evidence source_evidence_literature NP301576.RAyad_MYDbtVchUMZqg1pYhSHz3InoKWPp17ZLdh2hKwY130_provenance.
- NP301576.RAyad_MYDbtVchUMZqg1pYhSHz3InoKWPp17ZLdh2hKwY130_assertion SIO_000772 8847566 NP301576.RAyad_MYDbtVchUMZqg1pYhSHz3InoKWPp17ZLdh2hKwY130_provenance.
- NP301576.RAyad_MYDbtVchUMZqg1pYhSHz3InoKWPp17ZLdh2hKwY130_assertion wasDerivedFrom befree-20150227 NP301576.RAyad_MYDbtVchUMZqg1pYhSHz3InoKWPp17ZLdh2hKwY130_provenance.
- NP301576.RAyad_MYDbtVchUMZqg1pYhSHz3InoKWPp17ZLdh2hKwY130_assertion wasGeneratedBy ECO_0000203 NP301576.RAyad_MYDbtVchUMZqg1pYhSHz3InoKWPp17ZLdh2hKwY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP301576.RAyad_MYDbtVchUMZqg1pYhSHz3InoKWPp17ZLdh2hKwY130_provenance.