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- source_evidence_literature type ECO_0000212 NP258172.RAyTTVnYeN41Psxp081NKyDDgnWqltUus4-DCuHBjiGEA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP258172.RAyTTVnYeN41Psxp081NKyDDgnWqltUus4-DCuHBjiGEA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP258172.RAyTTVnYeN41Psxp081NKyDDgnWqltUus4-DCuHBjiGEA130_provenance.
- befree-2016 importedOn "2016-02-19" NP258172.RAyTTVnYeN41Psxp081NKyDDgnWqltUus4-DCuHBjiGEA130_provenance.
- NP258172.RAyTTVnYeN41Psxp081NKyDDgnWqltUus4-DCuHBjiGEA130_assertion wasGeneratedBy ECO_0000203 NP258172.RAyTTVnYeN41Psxp081NKyDDgnWqltUus4-DCuHBjiGEA130_provenance.
- NP258172.RAyTTVnYeN41Psxp081NKyDDgnWqltUus4-DCuHBjiGEA130_assertion wasDerivedFrom befree-2016 NP258172.RAyTTVnYeN41Psxp081NKyDDgnWqltUus4-DCuHBjiGEA130_provenance.
- NP258172.RAyTTVnYeN41Psxp081NKyDDgnWqltUus4-DCuHBjiGEA130_assertion SIO_000772 10414310 NP258172.RAyTTVnYeN41Psxp081NKyDDgnWqltUus4-DCuHBjiGEA130_provenance.
- NP258172.RAyTTVnYeN41Psxp081NKyDDgnWqltUus4-DCuHBjiGEA130_assertion evidence source_evidence_literature NP258172.RAyTTVnYeN41Psxp081NKyDDgnWqltUus4-DCuHBjiGEA130_provenance.
- NP258172.RAyTTVnYeN41Psxp081NKyDDgnWqltUus4-DCuHBjiGEA130_assertion description "[Mutations in KVLQT1 and HERG are the most common cause of LQT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258172.RAyTTVnYeN41Psxp081NKyDDgnWqltUus4-DCuHBjiGEA130_provenance.