Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP834898.RAujujjVsoo7vje5a0cIlukRgnOzHBiSKW1j8gl0z73X0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP834898.RAujujjVsoo7vje5a0cIlukRgnOzHBiSKW1j8gl0z73X0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP834898.RAujujjVsoo7vje5a0cIlukRgnOzHBiSKW1j8gl0z73X0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP834898.RAujujjVsoo7vje5a0cIlukRgnOzHBiSKW1j8gl0z73X0130_provenance.
- NP834898.RAujujjVsoo7vje5a0cIlukRgnOzHBiSKW1j8gl0z73X0130_assertion description "[Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP834898.RAujujjVsoo7vje5a0cIlukRgnOzHBiSKW1j8gl0z73X0130_provenance.
- NP834898.RAujujjVsoo7vje5a0cIlukRgnOzHBiSKW1j8gl0z73X0130_assertion evidence source_evidence_literature NP834898.RAujujjVsoo7vje5a0cIlukRgnOzHBiSKW1j8gl0z73X0130_provenance.
- NP834898.RAujujjVsoo7vje5a0cIlukRgnOzHBiSKW1j8gl0z73X0130_assertion SIO_000772 20736978 NP834898.RAujujjVsoo7vje5a0cIlukRgnOzHBiSKW1j8gl0z73X0130_provenance.
- NP834898.RAujujjVsoo7vje5a0cIlukRgnOzHBiSKW1j8gl0z73X0130_assertion wasDerivedFrom befree-2016 NP834898.RAujujjVsoo7vje5a0cIlukRgnOzHBiSKW1j8gl0z73X0130_provenance.
- NP834898.RAujujjVsoo7vje5a0cIlukRgnOzHBiSKW1j8gl0z73X0130_assertion wasGeneratedBy ECO_0000203 NP834898.RAujujjVsoo7vje5a0cIlukRgnOzHBiSKW1j8gl0z73X0130_provenance.
- befree-2016 importedOn "2016-02-19" NP834898.RAujujjVsoo7vje5a0cIlukRgnOzHBiSKW1j8gl0z73X0130_provenance.