Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP270395.RAGy3FYtH9hAoyYRDJ9kqWTAYaoaxEEhVeQsB-3hQ9HYA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP270395.RAGy3FYtH9hAoyYRDJ9kqWTAYaoaxEEhVeQsB-3hQ9HYA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP270395.RAGy3FYtH9hAoyYRDJ9kqWTAYaoaxEEhVeQsB-3hQ9HYA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP270395.RAGy3FYtH9hAoyYRDJ9kqWTAYaoaxEEhVeQsB-3hQ9HYA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP270395.RAGy3FYtH9hAoyYRDJ9kqWTAYaoaxEEhVeQsB-3hQ9HYA130_provenance.
- NP270395.RAGy3FYtH9hAoyYRDJ9kqWTAYaoaxEEhVeQsB-3hQ9HYA130_assertion wasGeneratedBy ECO_0000203 NP270395.RAGy3FYtH9hAoyYRDJ9kqWTAYaoaxEEhVeQsB-3hQ9HYA130_provenance.
- NP270395.RAGy3FYtH9hAoyYRDJ9kqWTAYaoaxEEhVeQsB-3hQ9HYA130_assertion wasDerivedFrom befree-20150227 NP270395.RAGy3FYtH9hAoyYRDJ9kqWTAYaoaxEEhVeQsB-3hQ9HYA130_provenance.
- NP270395.RAGy3FYtH9hAoyYRDJ9kqWTAYaoaxEEhVeQsB-3hQ9HYA130_assertion SIO_000772 18726931 NP270395.RAGy3FYtH9hAoyYRDJ9kqWTAYaoaxEEhVeQsB-3hQ9HYA130_provenance.
- NP270395.RAGy3FYtH9hAoyYRDJ9kqWTAYaoaxEEhVeQsB-3hQ9HYA130_assertion evidence source_evidence_literature NP270395.RAGy3FYtH9hAoyYRDJ9kqWTAYaoaxEEhVeQsB-3hQ9HYA130_provenance.
- NP270395.RAGy3FYtH9hAoyYRDJ9kqWTAYaoaxEEhVeQsB-3hQ9HYA130_assertion description "[Mutations in FOXL2 are known to cause blepharophimosis syndrome (BPES), an autosomal dominant eyelid malformation associated (type I) or not (type II) with ovarian dysfunction, leading to premature ovarian failure (POF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP270395.RAGy3FYtH9hAoyYRDJ9kqWTAYaoaxEEhVeQsB-3hQ9HYA130_provenance.