Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1338324.RANP8rH16_h9YJoNjQpWM7QaNiuD7SvJMcYFOV4QY1Jwk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1338324.RANP8rH16_h9YJoNjQpWM7QaNiuD7SvJMcYFOV4QY1Jwk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1338324.RANP8rH16_h9YJoNjQpWM7QaNiuD7SvJMcYFOV4QY1Jwk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1338324.RANP8rH16_h9YJoNjQpWM7QaNiuD7SvJMcYFOV4QY1Jwk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1338324.RANP8rH16_h9YJoNjQpWM7QaNiuD7SvJMcYFOV4QY1Jwk130_provenance.
- NP1338324.RANP8rH16_h9YJoNjQpWM7QaNiuD7SvJMcYFOV4QY1Jwk130_assertion wasGeneratedBy ECO_0000203 NP1338324.RANP8rH16_h9YJoNjQpWM7QaNiuD7SvJMcYFOV4QY1Jwk130_provenance.
- NP1338324.RANP8rH16_h9YJoNjQpWM7QaNiuD7SvJMcYFOV4QY1Jwk130_assertion wasDerivedFrom befree-2016 NP1338324.RANP8rH16_h9YJoNjQpWM7QaNiuD7SvJMcYFOV4QY1Jwk130_provenance.
- NP1338324.RANP8rH16_h9YJoNjQpWM7QaNiuD7SvJMcYFOV4QY1Jwk130_assertion SIO_000772 8308926 NP1338324.RANP8rH16_h9YJoNjQpWM7QaNiuD7SvJMcYFOV4QY1Jwk130_provenance.
- NP1338324.RANP8rH16_h9YJoNjQpWM7QaNiuD7SvJMcYFOV4QY1Jwk130_assertion evidence source_evidence_literature NP1338324.RANP8rH16_h9YJoNjQpWM7QaNiuD7SvJMcYFOV4QY1Jwk130_provenance.
- NP1338324.RANP8rH16_h9YJoNjQpWM7QaNiuD7SvJMcYFOV4QY1Jwk130_assertion description "[Germline p53 mutations are frequent in patients with multifocal glioma, glioma and another primary malignancy, and glioma associated with a family history of cancer, particularly if these factors are combined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1338324.RANP8rH16_h9YJoNjQpWM7QaNiuD7SvJMcYFOV4QY1Jwk130_provenance.