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- source_evidence_literature type ECO_0000212 NP780866.RAD6N0Ne1kmnWTrE8s-TndxwvdOi0MlUrmGW5r3LscvqU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP780866.RAD6N0Ne1kmnWTrE8s-TndxwvdOi0MlUrmGW5r3LscvqU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP780866.RAD6N0Ne1kmnWTrE8s-TndxwvdOi0MlUrmGW5r3LscvqU130_provenance.
- NP780866.RAD6N0Ne1kmnWTrE8s-TndxwvdOi0MlUrmGW5r3LscvqU130_assertion description "[X-ray repair cross-complementing group 4 (XRCC4) promoter -1394( *)T-related genotype, but not XRCC4 codon 247/intron 3 or xeroderma pigmentosum group D codon 312, 751/promoter -114, polymorphisms are correlated with higher susceptibility to myoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP780866.RAD6N0Ne1kmnWTrE8s-TndxwvdOi0MlUrmGW5r3LscvqU130_provenance.
- NP780866.RAD6N0Ne1kmnWTrE8s-TndxwvdOi0MlUrmGW5r3LscvqU130_assertion evidence source_evidence_literature NP780866.RAD6N0Ne1kmnWTrE8s-TndxwvdOi0MlUrmGW5r3LscvqU130_provenance.
- NP780866.RAD6N0Ne1kmnWTrE8s-TndxwvdOi0MlUrmGW5r3LscvqU130_assertion SIO_000772 18177646 NP780866.RAD6N0Ne1kmnWTrE8s-TndxwvdOi0MlUrmGW5r3LscvqU130_provenance.
- NP780866.RAD6N0Ne1kmnWTrE8s-TndxwvdOi0MlUrmGW5r3LscvqU130_assertion wasDerivedFrom befree-20150227 NP780866.RAD6N0Ne1kmnWTrE8s-TndxwvdOi0MlUrmGW5r3LscvqU130_provenance.
- NP780866.RAD6N0Ne1kmnWTrE8s-TndxwvdOi0MlUrmGW5r3LscvqU130_assertion wasGeneratedBy ECO_0000203 NP780866.RAD6N0Ne1kmnWTrE8s-TndxwvdOi0MlUrmGW5r3LscvqU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP780866.RAD6N0Ne1kmnWTrE8s-TndxwvdOi0MlUrmGW5r3LscvqU130_provenance.