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- source_evidence_literature type ECO_0000212 NP520870.RAAfC08Ae24jw5yCsrGTi6CrHf5Yg1GRX_iCOu74wDQ18130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP520870.RAAfC08Ae24jw5yCsrGTi6CrHf5Yg1GRX_iCOu74wDQ18130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP520870.RAAfC08Ae24jw5yCsrGTi6CrHf5Yg1GRX_iCOu74wDQ18130_provenance.
- befree-20150227 importedOn "2015-02-27" NP520870.RAAfC08Ae24jw5yCsrGTi6CrHf5Yg1GRX_iCOu74wDQ18130_provenance.
- NP520870.RAAfC08Ae24jw5yCsrGTi6CrHf5Yg1GRX_iCOu74wDQ18130_assertion wasGeneratedBy ECO_0000203 NP520870.RAAfC08Ae24jw5yCsrGTi6CrHf5Yg1GRX_iCOu74wDQ18130_provenance.
- NP520870.RAAfC08Ae24jw5yCsrGTi6CrHf5Yg1GRX_iCOu74wDQ18130_assertion wasDerivedFrom befree-20150227 NP520870.RAAfC08Ae24jw5yCsrGTi6CrHf5Yg1GRX_iCOu74wDQ18130_provenance.
- NP520870.RAAfC08Ae24jw5yCsrGTi6CrHf5Yg1GRX_iCOu74wDQ18130_assertion SIO_000772 24031091 NP520870.RAAfC08Ae24jw5yCsrGTi6CrHf5Yg1GRX_iCOu74wDQ18130_provenance.
- NP520870.RAAfC08Ae24jw5yCsrGTi6CrHf5Yg1GRX_iCOu74wDQ18130_assertion evidence source_evidence_literature NP520870.RAAfC08Ae24jw5yCsrGTi6CrHf5Yg1GRX_iCOu74wDQ18130_provenance.
- NP520870.RAAfC08Ae24jw5yCsrGTi6CrHf5Yg1GRX_iCOu74wDQ18130_assertion description "[Diverse mutations in PROKR2, a gene involved both in monogenic recessive and digenic/oligogenic KS transmission modes, were found in 23.3% of the Maghrebian patients, but only in 5.1% of the European patients (Fisher's exact test, P<0.001), whereas mutations in each of the other four KS genes were present either at similar frequencies in the Maghrebian and European patients (KAL1, PROK2, FGF8, from 6.6 to 0.8%; Fisher's exact test, P>0.4 for all comparisons) or at a lower frequency in Maghrebian patients (FGFR1, 5.0 vs 11.7%; Fisher's exact test, P<0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP520870.RAAfC08Ae24jw5yCsrGTi6CrHf5Yg1GRX_iCOu74wDQ18130_provenance.