Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP357834.RACQwYfBfs6WQ2SCgu_0PlPTMS_6mEzkTssIuEE51Qat0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP357834.RACQwYfBfs6WQ2SCgu_0PlPTMS_6mEzkTssIuEE51Qat0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP357834.RACQwYfBfs6WQ2SCgu_0PlPTMS_6mEzkTssIuEE51Qat0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP357834.RACQwYfBfs6WQ2SCgu_0PlPTMS_6mEzkTssIuEE51Qat0130_provenance.
- NP357834.RACQwYfBfs6WQ2SCgu_0PlPTMS_6mEzkTssIuEE51Qat0130_assertion description "[In contrast to recently published FISH results, we only detected heterozygous p53 deletions in eight out of the 74 patients, three of them showing a monosomy 17.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357834.RACQwYfBfs6WQ2SCgu_0PlPTMS_6mEzkTssIuEE51Qat0130_provenance.
- NP357834.RACQwYfBfs6WQ2SCgu_0PlPTMS_6mEzkTssIuEE51Qat0130_assertion evidence source_evidence_literature NP357834.RACQwYfBfs6WQ2SCgu_0PlPTMS_6mEzkTssIuEE51Qat0130_provenance.
- NP357834.RACQwYfBfs6WQ2SCgu_0PlPTMS_6mEzkTssIuEE51Qat0130_assertion SIO_000772 10602435 NP357834.RACQwYfBfs6WQ2SCgu_0PlPTMS_6mEzkTssIuEE51Qat0130_provenance.
- NP357834.RACQwYfBfs6WQ2SCgu_0PlPTMS_6mEzkTssIuEE51Qat0130_assertion wasDerivedFrom befree-20140225 NP357834.RACQwYfBfs6WQ2SCgu_0PlPTMS_6mEzkTssIuEE51Qat0130_provenance.
- NP357834.RACQwYfBfs6WQ2SCgu_0PlPTMS_6mEzkTssIuEE51Qat0130_assertion wasGeneratedBy ECO_0000203 NP357834.RACQwYfBfs6WQ2SCgu_0PlPTMS_6mEzkTssIuEE51Qat0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP357834.RACQwYfBfs6WQ2SCgu_0PlPTMS_6mEzkTssIuEE51Qat0130_provenance.