Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP270319.RACyMtH3TRrvEHAYaNaR6gd7x_38OGiSb5R9RYJXNWF8g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP270319.RACyMtH3TRrvEHAYaNaR6gd7x_38OGiSb5R9RYJXNWF8g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP270319.RACyMtH3TRrvEHAYaNaR6gd7x_38OGiSb5R9RYJXNWF8g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP270319.RACyMtH3TRrvEHAYaNaR6gd7x_38OGiSb5R9RYJXNWF8g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP270319.RACyMtH3TRrvEHAYaNaR6gd7x_38OGiSb5R9RYJXNWF8g130_provenance.
- NP270319.RACyMtH3TRrvEHAYaNaR6gd7x_38OGiSb5R9RYJXNWF8g130_assertion wasGeneratedBy ECO_0000203 NP270319.RACyMtH3TRrvEHAYaNaR6gd7x_38OGiSb5R9RYJXNWF8g130_provenance.
- NP270319.RACyMtH3TRrvEHAYaNaR6gd7x_38OGiSb5R9RYJXNWF8g130_assertion wasDerivedFrom befree-20150227 NP270319.RACyMtH3TRrvEHAYaNaR6gd7x_38OGiSb5R9RYJXNWF8g130_provenance.
- NP270319.RACyMtH3TRrvEHAYaNaR6gd7x_38OGiSb5R9RYJXNWF8g130_assertion SIO_000772 18726931 NP270319.RACyMtH3TRrvEHAYaNaR6gd7x_38OGiSb5R9RYJXNWF8g130_provenance.
- NP270319.RACyMtH3TRrvEHAYaNaR6gd7x_38OGiSb5R9RYJXNWF8g130_assertion evidence source_evidence_literature NP270319.RACyMtH3TRrvEHAYaNaR6gd7x_38OGiSb5R9RYJXNWF8g130_provenance.
- NP270319.RACyMtH3TRrvEHAYaNaR6gd7x_38OGiSb5R9RYJXNWF8g130_assertion description "[The FOXL2 gene is one of 10 forkhead genes, the mutations of which lead to human developmental disorders, often with ocular manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP270319.RACyMtH3TRrvEHAYaNaR6gd7x_38OGiSb5R9RYJXNWF8g130_provenance.