Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP270319.RACyMtH3TRrvEHAYaNaR6gd7x_38OGiSb5R9RYJXNWF8g130_assertion> ?p ?o ?g. }
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- NP270319.RACyMtH3TRrvEHAYaNaR6gd7x_38OGiSb5R9RYJXNWF8g130_assertion type Assertion NP270319.RACyMtH3TRrvEHAYaNaR6gd7x_38OGiSb5R9RYJXNWF8g130_head.
- 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.