Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP209946.RA4rzpXzGjecaYtCs7qIpKNEDMXlsDUpNENHjwkWuDbpQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP209946.RA4rzpXzGjecaYtCs7qIpKNEDMXlsDUpNENHjwkWuDbpQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP209946.RA4rzpXzGjecaYtCs7qIpKNEDMXlsDUpNENHjwkWuDbpQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP209946.RA4rzpXzGjecaYtCs7qIpKNEDMXlsDUpNENHjwkWuDbpQ130_provenance.
- NP209946.RA4rzpXzGjecaYtCs7qIpKNEDMXlsDUpNENHjwkWuDbpQ130_assertion wasGeneratedBy ECO_0000203 NP209946.RA4rzpXzGjecaYtCs7qIpKNEDMXlsDUpNENHjwkWuDbpQ130_provenance.
- NP209946.RA4rzpXzGjecaYtCs7qIpKNEDMXlsDUpNENHjwkWuDbpQ130_assertion wasDerivedFrom befree-20140225 NP209946.RA4rzpXzGjecaYtCs7qIpKNEDMXlsDUpNENHjwkWuDbpQ130_provenance.
- NP209946.RA4rzpXzGjecaYtCs7qIpKNEDMXlsDUpNENHjwkWuDbpQ130_assertion SIO_000772 10850866 NP209946.RA4rzpXzGjecaYtCs7qIpKNEDMXlsDUpNENHjwkWuDbpQ130_provenance.
- NP209946.RA4rzpXzGjecaYtCs7qIpKNEDMXlsDUpNENHjwkWuDbpQ130_assertion evidence source_evidence_literature NP209946.RA4rzpXzGjecaYtCs7qIpKNEDMXlsDUpNENHjwkWuDbpQ130_provenance.
- NP209946.RA4rzpXzGjecaYtCs7qIpKNEDMXlsDUpNENHjwkWuDbpQ130_assertion description "[Primary glioblastomas are characterized by EGFR amplification/overexpression, PTEN mutation, homozygous p16 deletion, and loss of heterozygosity (LOH) on entire chromosome 10, whereas secondary glioblastomas frequently contain p53 mutations and show LOH on chromosome 10q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209946.RA4rzpXzGjecaYtCs7qIpKNEDMXlsDUpNENHjwkWuDbpQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP209946.RA4rzpXzGjecaYtCs7qIpKNEDMXlsDUpNENHjwkWuDbpQ130_provenance.