Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP918833.RAzV7KnA37R5yv3tOwX5ylBKhCsNWRDyK6iPia2dwFNX8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP918833.RAzV7KnA37R5yv3tOwX5ylBKhCsNWRDyK6iPia2dwFNX8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP918833.RAzV7KnA37R5yv3tOwX5ylBKhCsNWRDyK6iPia2dwFNX8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP918833.RAzV7KnA37R5yv3tOwX5ylBKhCsNWRDyK6iPia2dwFNX8130_provenance.
- NP918833.RAzV7KnA37R5yv3tOwX5ylBKhCsNWRDyK6iPia2dwFNX8130_assertion description "[Premature ovarian failure in the autosomal dominant disorder blepharophimosis-ptosis-epicanthus inversus is due to mutations in the gene encoding Forkhead L2 (FOXL2), producing putative truncated proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918833.RAzV7KnA37R5yv3tOwX5ylBKhCsNWRDyK6iPia2dwFNX8130_provenance.
- NP918833.RAzV7KnA37R5yv3tOwX5ylBKhCsNWRDyK6iPia2dwFNX8130_assertion evidence source_evidence_literature NP918833.RAzV7KnA37R5yv3tOwX5ylBKhCsNWRDyK6iPia2dwFNX8130_provenance.
- NP918833.RAzV7KnA37R5yv3tOwX5ylBKhCsNWRDyK6iPia2dwFNX8130_assertion SIO_000772 21862621 NP918833.RAzV7KnA37R5yv3tOwX5ylBKhCsNWRDyK6iPia2dwFNX8130_provenance.
- NP918833.RAzV7KnA37R5yv3tOwX5ylBKhCsNWRDyK6iPia2dwFNX8130_assertion wasDerivedFrom befree-2016 NP918833.RAzV7KnA37R5yv3tOwX5ylBKhCsNWRDyK6iPia2dwFNX8130_provenance.
- NP918833.RAzV7KnA37R5yv3tOwX5ylBKhCsNWRDyK6iPia2dwFNX8130_assertion wasGeneratedBy ECO_0000203 NP918833.RAzV7KnA37R5yv3tOwX5ylBKhCsNWRDyK6iPia2dwFNX8130_provenance.
- befree-2016 importedOn "2016-02-19" NP918833.RAzV7KnA37R5yv3tOwX5ylBKhCsNWRDyK6iPia2dwFNX8130_provenance.