Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP474229.RAiBwgg6APoMs7n2zAPFKJzX3hukZZyrIqzNuSDEGGGP0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP474229.RAiBwgg6APoMs7n2zAPFKJzX3hukZZyrIqzNuSDEGGGP0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP474229.RAiBwgg6APoMs7n2zAPFKJzX3hukZZyrIqzNuSDEGGGP0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP474229.RAiBwgg6APoMs7n2zAPFKJzX3hukZZyrIqzNuSDEGGGP0130_provenance.
- NP474229.RAiBwgg6APoMs7n2zAPFKJzX3hukZZyrIqzNuSDEGGGP0130_assertion description "[A p53 missense mutation was detected at codon 161 (GCC-->ACC, Ala-->Thr) in only one oligoastrocytoma without allelic loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP474229.RAiBwgg6APoMs7n2zAPFKJzX3hukZZyrIqzNuSDEGGGP0130_provenance.
- NP474229.RAiBwgg6APoMs7n2zAPFKJzX3hukZZyrIqzNuSDEGGGP0130_assertion evidence source_evidence_literature NP474229.RAiBwgg6APoMs7n2zAPFKJzX3hukZZyrIqzNuSDEGGGP0130_provenance.
- NP474229.RAiBwgg6APoMs7n2zAPFKJzX3hukZZyrIqzNuSDEGGGP0130_assertion SIO_000772 12507133 NP474229.RAiBwgg6APoMs7n2zAPFKJzX3hukZZyrIqzNuSDEGGGP0130_provenance.
- NP474229.RAiBwgg6APoMs7n2zAPFKJzX3hukZZyrIqzNuSDEGGGP0130_assertion wasDerivedFrom befree-20140225 NP474229.RAiBwgg6APoMs7n2zAPFKJzX3hukZZyrIqzNuSDEGGGP0130_provenance.
- NP474229.RAiBwgg6APoMs7n2zAPFKJzX3hukZZyrIqzNuSDEGGGP0130_assertion wasGeneratedBy ECO_0000203 NP474229.RAiBwgg6APoMs7n2zAPFKJzX3hukZZyrIqzNuSDEGGGP0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP474229.RAiBwgg6APoMs7n2zAPFKJzX3hukZZyrIqzNuSDEGGGP0130_provenance.