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- source_evidence_literature type ECO_0000212 NP1293478.RAoanUgcYdBu-WhSrWPsto8RzEypuNteWQwsbHHdTk-1g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293478.RAoanUgcYdBu-WhSrWPsto8RzEypuNteWQwsbHHdTk-1g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293478.RAoanUgcYdBu-WhSrWPsto8RzEypuNteWQwsbHHdTk-1g130_provenance.
- NP1293478.RAoanUgcYdBu-WhSrWPsto8RzEypuNteWQwsbHHdTk-1g130_assertion description "[Mutations in the forkhead box L2 (FOXL2) gene cause two types of BPES distinguished by the presence (type I) and absence (type II) of premature ovarian failure (POF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293478.RAoanUgcYdBu-WhSrWPsto8RzEypuNteWQwsbHHdTk-1g130_provenance.
- NP1293478.RAoanUgcYdBu-WhSrWPsto8RzEypuNteWQwsbHHdTk-1g130_assertion evidence source_evidence_literature NP1293478.RAoanUgcYdBu-WhSrWPsto8RzEypuNteWQwsbHHdTk-1g130_provenance.
- NP1293478.RAoanUgcYdBu-WhSrWPsto8RzEypuNteWQwsbHHdTk-1g130_assertion SIO_000772 26323275 NP1293478.RAoanUgcYdBu-WhSrWPsto8RzEypuNteWQwsbHHdTk-1g130_provenance.
- NP1293478.RAoanUgcYdBu-WhSrWPsto8RzEypuNteWQwsbHHdTk-1g130_assertion wasDerivedFrom befree-2016 NP1293478.RAoanUgcYdBu-WhSrWPsto8RzEypuNteWQwsbHHdTk-1g130_provenance.
- NP1293478.RAoanUgcYdBu-WhSrWPsto8RzEypuNteWQwsbHHdTk-1g130_assertion wasGeneratedBy ECO_0000203 NP1293478.RAoanUgcYdBu-WhSrWPsto8RzEypuNteWQwsbHHdTk-1g130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293478.RAoanUgcYdBu-WhSrWPsto8RzEypuNteWQwsbHHdTk-1g130_provenance.