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- source_evidence_literature type ECO_0000212 NP932047.RA02sepjAw1fYjKqN3i_lNo6RhcAYtQoyBauBbyO9gfQE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP932047.RA02sepjAw1fYjKqN3i_lNo6RhcAYtQoyBauBbyO9gfQE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP932047.RA02sepjAw1fYjKqN3i_lNo6RhcAYtQoyBauBbyO9gfQE130_provenance.
- NP932047.RA02sepjAw1fYjKqN3i_lNo6RhcAYtQoyBauBbyO9gfQE130_assertion description "[Recently, missense and truncating mutations in the gene PCDH19 have been reported to cause female-restricted epilepsy with mental retardation (EFMR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932047.RA02sepjAw1fYjKqN3i_lNo6RhcAYtQoyBauBbyO9gfQE130_provenance.
- NP932047.RA02sepjAw1fYjKqN3i_lNo6RhcAYtQoyBauBbyO9gfQE130_assertion evidence source_evidence_literature NP932047.RA02sepjAw1fYjKqN3i_lNo6RhcAYtQoyBauBbyO9gfQE130_provenance.
- NP932047.RA02sepjAw1fYjKqN3i_lNo6RhcAYtQoyBauBbyO9gfQE130_assertion SIO_000772 22091964 NP932047.RA02sepjAw1fYjKqN3i_lNo6RhcAYtQoyBauBbyO9gfQE130_provenance.
- NP932047.RA02sepjAw1fYjKqN3i_lNo6RhcAYtQoyBauBbyO9gfQE130_assertion wasDerivedFrom befree-20150227 NP932047.RA02sepjAw1fYjKqN3i_lNo6RhcAYtQoyBauBbyO9gfQE130_provenance.
- NP932047.RA02sepjAw1fYjKqN3i_lNo6RhcAYtQoyBauBbyO9gfQE130_assertion wasGeneratedBy ECO_0000203 NP932047.RA02sepjAw1fYjKqN3i_lNo6RhcAYtQoyBauBbyO9gfQE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP932047.RA02sepjAw1fYjKqN3i_lNo6RhcAYtQoyBauBbyO9gfQE130_provenance.