Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1110128.RAUrJ4ud03MGOHPKdQPrL2CTqtpulPu3PEGRvpB4scaCI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1110128.RAUrJ4ud03MGOHPKdQPrL2CTqtpulPu3PEGRvpB4scaCI130_assertion type Assertion NP1110128.RAUrJ4ud03MGOHPKdQPrL2CTqtpulPu3PEGRvpB4scaCI130_head.
- NP1110128.RAUrJ4ud03MGOHPKdQPrL2CTqtpulPu3PEGRvpB4scaCI130_assertion wasGeneratedBy ECO_0000203 NP1110128.RAUrJ4ud03MGOHPKdQPrL2CTqtpulPu3PEGRvpB4scaCI130_provenance.
- NP1110128.RAUrJ4ud03MGOHPKdQPrL2CTqtpulPu3PEGRvpB4scaCI130_assertion wasDerivedFrom befree-2016 NP1110128.RAUrJ4ud03MGOHPKdQPrL2CTqtpulPu3PEGRvpB4scaCI130_provenance.
- NP1110128.RAUrJ4ud03MGOHPKdQPrL2CTqtpulPu3PEGRvpB4scaCI130_assertion SIO_000772 24031091 NP1110128.RAUrJ4ud03MGOHPKdQPrL2CTqtpulPu3PEGRvpB4scaCI130_provenance.
- NP1110128.RAUrJ4ud03MGOHPKdQPrL2CTqtpulPu3PEGRvpB4scaCI130_assertion evidence source_evidence_literature NP1110128.RAUrJ4ud03MGOHPKdQPrL2CTqtpulPu3PEGRvpB4scaCI130_provenance.
- NP1110128.RAUrJ4ud03MGOHPKdQPrL2CTqtpulPu3PEGRvpB4scaCI130_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." NP1110128.RAUrJ4ud03MGOHPKdQPrL2CTqtpulPu3PEGRvpB4scaCI130_provenance.