Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP500122.RAXHPWMVcbIBBhavS-fSnOVUqI_M4XHpPTKwvC6f4KLK4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP500122.RAXHPWMVcbIBBhavS-fSnOVUqI_M4XHpPTKwvC6f4KLK4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP500122.RAXHPWMVcbIBBhavS-fSnOVUqI_M4XHpPTKwvC6f4KLK4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP500122.RAXHPWMVcbIBBhavS-fSnOVUqI_M4XHpPTKwvC6f4KLK4130_provenance.
- NP500122.RAXHPWMVcbIBBhavS-fSnOVUqI_M4XHpPTKwvC6f4KLK4130_assertion wasGeneratedBy ECO_0000203 NP500122.RAXHPWMVcbIBBhavS-fSnOVUqI_M4XHpPTKwvC6f4KLK4130_provenance.
- NP500122.RAXHPWMVcbIBBhavS-fSnOVUqI_M4XHpPTKwvC6f4KLK4130_assertion wasDerivedFrom befree-20140225 NP500122.RAXHPWMVcbIBBhavS-fSnOVUqI_M4XHpPTKwvC6f4KLK4130_provenance.
- NP500122.RAXHPWMVcbIBBhavS-fSnOVUqI_M4XHpPTKwvC6f4KLK4130_assertion SIO_000772 18726931 NP500122.RAXHPWMVcbIBBhavS-fSnOVUqI_M4XHpPTKwvC6f4KLK4130_provenance.
- NP500122.RAXHPWMVcbIBBhavS-fSnOVUqI_M4XHpPTKwvC6f4KLK4130_assertion evidence source_evidence_literature NP500122.RAXHPWMVcbIBBhavS-fSnOVUqI_M4XHpPTKwvC6f4KLK4130_provenance.
- NP500122.RAXHPWMVcbIBBhavS-fSnOVUqI_M4XHpPTKwvC6f4KLK4130_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." NP500122.RAXHPWMVcbIBBhavS-fSnOVUqI_M4XHpPTKwvC6f4KLK4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP500122.RAXHPWMVcbIBBhavS-fSnOVUqI_M4XHpPTKwvC6f4KLK4130_provenance.