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- source_evidence_literature type ECO_0000212 NP1012165.RAr6MICdEX_02N3Bh7Sf5BpMO3r_um3arhluDPwTBsTxg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1012165.RAr6MICdEX_02N3Bh7Sf5BpMO3r_um3arhluDPwTBsTxg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1012165.RAr6MICdEX_02N3Bh7Sf5BpMO3r_um3arhluDPwTBsTxg130_provenance.
- NP1012165.RAr6MICdEX_02N3Bh7Sf5BpMO3r_um3arhluDPwTBsTxg130_assertion description "[Mutations in the CDKL5 gene have been associated with the early-onset seizure variant of Rett syndrome and mutations in FOXG1 have been associated with the congenital Rett syndrome variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1012165.RAr6MICdEX_02N3Bh7Sf5BpMO3r_um3arhluDPwTBsTxg130_provenance.
- NP1012165.RAr6MICdEX_02N3Bh7Sf5BpMO3r_um3arhluDPwTBsTxg130_assertion evidence source_evidence_literature NP1012165.RAr6MICdEX_02N3Bh7Sf5BpMO3r_um3arhluDPwTBsTxg130_provenance.
- NP1012165.RAr6MICdEX_02N3Bh7Sf5BpMO3r_um3arhluDPwTBsTxg130_assertion SIO_000772 22968132 NP1012165.RAr6MICdEX_02N3Bh7Sf5BpMO3r_um3arhluDPwTBsTxg130_provenance.
- NP1012165.RAr6MICdEX_02N3Bh7Sf5BpMO3r_um3arhluDPwTBsTxg130_assertion wasDerivedFrom befree-2016 NP1012165.RAr6MICdEX_02N3Bh7Sf5BpMO3r_um3arhluDPwTBsTxg130_provenance.
- NP1012165.RAr6MICdEX_02N3Bh7Sf5BpMO3r_um3arhluDPwTBsTxg130_assertion wasGeneratedBy ECO_0000203 NP1012165.RAr6MICdEX_02N3Bh7Sf5BpMO3r_um3arhluDPwTBsTxg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1012165.RAr6MICdEX_02N3Bh7Sf5BpMO3r_um3arhluDPwTBsTxg130_provenance.