Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP825967.RArcMFBJgSg5ly92QFOVER3a0ECjpiwtYWbub2X0Vwl5I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP825967.RArcMFBJgSg5ly92QFOVER3a0ECjpiwtYWbub2X0Vwl5I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP825967.RArcMFBJgSg5ly92QFOVER3a0ECjpiwtYWbub2X0Vwl5I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP825967.RArcMFBJgSg5ly92QFOVER3a0ECjpiwtYWbub2X0Vwl5I130_provenance.
- NP825967.RArcMFBJgSg5ly92QFOVER3a0ECjpiwtYWbub2X0Vwl5I130_assertion wasGeneratedBy ECO_0000203 NP825967.RArcMFBJgSg5ly92QFOVER3a0ECjpiwtYWbub2X0Vwl5I130_provenance.
- NP825967.RArcMFBJgSg5ly92QFOVER3a0ECjpiwtYWbub2X0Vwl5I130_assertion wasDerivedFrom befree-20140225 NP825967.RArcMFBJgSg5ly92QFOVER3a0ECjpiwtYWbub2X0Vwl5I130_provenance.
- NP825967.RArcMFBJgSg5ly92QFOVER3a0ECjpiwtYWbub2X0Vwl5I130_assertion SIO_000772 18726931 NP825967.RArcMFBJgSg5ly92QFOVER3a0ECjpiwtYWbub2X0Vwl5I130_provenance.
- NP825967.RArcMFBJgSg5ly92QFOVER3a0ECjpiwtYWbub2X0Vwl5I130_assertion evidence source_evidence_literature NP825967.RArcMFBJgSg5ly92QFOVER3a0ECjpiwtYWbub2X0Vwl5I130_provenance.
- NP825967.RArcMFBJgSg5ly92QFOVER3a0ECjpiwtYWbub2X0Vwl5I130_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." NP825967.RArcMFBJgSg5ly92QFOVER3a0ECjpiwtYWbub2X0Vwl5I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP825967.RArcMFBJgSg5ly92QFOVER3a0ECjpiwtYWbub2X0Vwl5I130_provenance.