Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP250838.RA3x8z4PPfUCXidFDXo0hyAnIguY93JzKl4gydKhmZb-c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP250838.RA3x8z4PPfUCXidFDXo0hyAnIguY93JzKl4gydKhmZb-c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP250838.RA3x8z4PPfUCXidFDXo0hyAnIguY93JzKl4gydKhmZb-c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP250838.RA3x8z4PPfUCXidFDXo0hyAnIguY93JzKl4gydKhmZb-c130_provenance.
- NP250838.RA3x8z4PPfUCXidFDXo0hyAnIguY93JzKl4gydKhmZb-c130_assertion description "[The p73 gene is monoallelically expressed in normal tissue, maps to chromosome 1p36 and is deleted in human neuroblastoma cell lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP250838.RA3x8z4PPfUCXidFDXo0hyAnIguY93JzKl4gydKhmZb-c130_provenance.
- NP250838.RA3x8z4PPfUCXidFDXo0hyAnIguY93JzKl4gydKhmZb-c130_assertion evidence source_evidence_literature NP250838.RA3x8z4PPfUCXidFDXo0hyAnIguY93JzKl4gydKhmZb-c130_provenance.
- NP250838.RA3x8z4PPfUCXidFDXo0hyAnIguY93JzKl4gydKhmZb-c130_assertion SIO_000772 10213163 NP250838.RA3x8z4PPfUCXidFDXo0hyAnIguY93JzKl4gydKhmZb-c130_provenance.
- NP250838.RA3x8z4PPfUCXidFDXo0hyAnIguY93JzKl4gydKhmZb-c130_assertion wasDerivedFrom befree-2016 NP250838.RA3x8z4PPfUCXidFDXo0hyAnIguY93JzKl4gydKhmZb-c130_provenance.
- NP250838.RA3x8z4PPfUCXidFDXo0hyAnIguY93JzKl4gydKhmZb-c130_assertion wasGeneratedBy ECO_0000203 NP250838.RA3x8z4PPfUCXidFDXo0hyAnIguY93JzKl4gydKhmZb-c130_provenance.
- befree-2016 importedOn "2016-02-19" NP250838.RA3x8z4PPfUCXidFDXo0hyAnIguY93JzKl4gydKhmZb-c130_provenance.