Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP834891.RAA4F95OP2oudEa5hOJNrCZIjTeSMiMUc8alXSLQ7PfSY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP834891.RAA4F95OP2oudEa5hOJNrCZIjTeSMiMUc8alXSLQ7PfSY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP834891.RAA4F95OP2oudEa5hOJNrCZIjTeSMiMUc8alXSLQ7PfSY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP834891.RAA4F95OP2oudEa5hOJNrCZIjTeSMiMUc8alXSLQ7PfSY130_provenance.
- NP834891.RAA4F95OP2oudEa5hOJNrCZIjTeSMiMUc8alXSLQ7PfSY130_assertion wasGeneratedBy ECO_0000203 NP834891.RAA4F95OP2oudEa5hOJNrCZIjTeSMiMUc8alXSLQ7PfSY130_provenance.
- NP834891.RAA4F95OP2oudEa5hOJNrCZIjTeSMiMUc8alXSLQ7PfSY130_assertion wasDerivedFrom befree-20140225 NP834891.RAA4F95OP2oudEa5hOJNrCZIjTeSMiMUc8alXSLQ7PfSY130_provenance.
- NP834891.RAA4F95OP2oudEa5hOJNrCZIjTeSMiMUc8alXSLQ7PfSY130_assertion SIO_000772 11181572 NP834891.RAA4F95OP2oudEa5hOJNrCZIjTeSMiMUc8alXSLQ7PfSY130_provenance.
- NP834891.RAA4F95OP2oudEa5hOJNrCZIjTeSMiMUc8alXSLQ7PfSY130_assertion evidence source_evidence_literature NP834891.RAA4F95OP2oudEa5hOJNrCZIjTeSMiMUc8alXSLQ7PfSY130_provenance.
- NP834891.RAA4F95OP2oudEa5hOJNrCZIjTeSMiMUc8alXSLQ7PfSY130_assertion description "[FGD1, the gene responsible for the inherited disease faciogenital dysplasia, encodes a guanine nucleotide exchange factor (GEF) that specifically activates the p21 GTPase Cdc42.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP834891.RAA4F95OP2oudEa5hOJNrCZIjTeSMiMUc8alXSLQ7PfSY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP834891.RAA4F95OP2oudEa5hOJNrCZIjTeSMiMUc8alXSLQ7PfSY130_provenance.