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- source_evidence_literature type ECO_0000212 NP623709.RANEDqMzI0z8_Juer2c5v7uBwJMp8EJ2OFPfSSmG8bi3s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP623709.RANEDqMzI0z8_Juer2c5v7uBwJMp8EJ2OFPfSSmG8bi3s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP623709.RANEDqMzI0z8_Juer2c5v7uBwJMp8EJ2OFPfSSmG8bi3s130_provenance.
- NP623709.RANEDqMzI0z8_Juer2c5v7uBwJMp8EJ2OFPfSSmG8bi3s130_assertion description "[Screening of the LGI4 coding region in BFIC and childhood absence epilepsy (CAE) revealed several frequent exonic polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623709.RANEDqMzI0z8_Juer2c5v7uBwJMp8EJ2OFPfSSmG8bi3s130_provenance.
- NP623709.RANEDqMzI0z8_Juer2c5v7uBwJMp8EJ2OFPfSSmG8bi3s130_assertion evidence source_evidence_literature NP623709.RANEDqMzI0z8_Juer2c5v7uBwJMp8EJ2OFPfSSmG8bi3s130_provenance.
- NP623709.RANEDqMzI0z8_Juer2c5v7uBwJMp8EJ2OFPfSSmG8bi3s130_assertion SIO_000772 14505228 NP623709.RANEDqMzI0z8_Juer2c5v7uBwJMp8EJ2OFPfSSmG8bi3s130_provenance.
- NP623709.RANEDqMzI0z8_Juer2c5v7uBwJMp8EJ2OFPfSSmG8bi3s130_assertion wasDerivedFrom befree-20140225 NP623709.RANEDqMzI0z8_Juer2c5v7uBwJMp8EJ2OFPfSSmG8bi3s130_provenance.
- NP623709.RANEDqMzI0z8_Juer2c5v7uBwJMp8EJ2OFPfSSmG8bi3s130_assertion wasGeneratedBy ECO_0000203 NP623709.RANEDqMzI0z8_Juer2c5v7uBwJMp8EJ2OFPfSSmG8bi3s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP623709.RANEDqMzI0z8_Juer2c5v7uBwJMp8EJ2OFPfSSmG8bi3s130_provenance.