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- source_evidence_literature type ECO_0000212 NP749336.RACDr3BNHeFMt_iE2NqwGhecnNvfXhk7qw7bOZtV0ClRk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP749336.RACDr3BNHeFMt_iE2NqwGhecnNvfXhk7qw7bOZtV0ClRk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP749336.RACDr3BNHeFMt_iE2NqwGhecnNvfXhk7qw7bOZtV0ClRk130_provenance.
- NP749336.RACDr3BNHeFMt_iE2NqwGhecnNvfXhk7qw7bOZtV0ClRk130_assertion description "[All the other loci analyzed were altered in less than 40% of cases and some of them (D3S1312, D3S1300, IFNA, D9S164, D13S176 and TP53) did not show alterations in any of the ameloblastomas analyzed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749336.RACDr3BNHeFMt_iE2NqwGhecnNvfXhk7qw7bOZtV0ClRk130_provenance.
- NP749336.RACDr3BNHeFMt_iE2NqwGhecnNvfXhk7qw7bOZtV0ClRk130_assertion evidence source_evidence_literature NP749336.RACDr3BNHeFMt_iE2NqwGhecnNvfXhk7qw7bOZtV0ClRk130_provenance.
- NP749336.RACDr3BNHeFMt_iE2NqwGhecnNvfXhk7qw7bOZtV0ClRk130_assertion SIO_000772 17307020 NP749336.RACDr3BNHeFMt_iE2NqwGhecnNvfXhk7qw7bOZtV0ClRk130_provenance.
- NP749336.RACDr3BNHeFMt_iE2NqwGhecnNvfXhk7qw7bOZtV0ClRk130_assertion wasDerivedFrom befree-20150227 NP749336.RACDr3BNHeFMt_iE2NqwGhecnNvfXhk7qw7bOZtV0ClRk130_provenance.
- NP749336.RACDr3BNHeFMt_iE2NqwGhecnNvfXhk7qw7bOZtV0ClRk130_assertion wasGeneratedBy ECO_0000203 NP749336.RACDr3BNHeFMt_iE2NqwGhecnNvfXhk7qw7bOZtV0ClRk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP749336.RACDr3BNHeFMt_iE2NqwGhecnNvfXhk7qw7bOZtV0ClRk130_provenance.