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- source_evidence_literature type ECO_0000212 NP78788.RA8rCBVxzOpgXLE7-bZWsav6we5T40g6eBk3Mc1nFPPSU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP78788.RA8rCBVxzOpgXLE7-bZWsav6we5T40g6eBk3Mc1nFPPSU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP78788.RA8rCBVxzOpgXLE7-bZWsav6we5T40g6eBk3Mc1nFPPSU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP78788.RA8rCBVxzOpgXLE7-bZWsav6we5T40g6eBk3Mc1nFPPSU130_provenance.
- NP78788.RA8rCBVxzOpgXLE7-bZWsav6we5T40g6eBk3Mc1nFPPSU130_assertion wasGeneratedBy ECO_0000203 NP78788.RA8rCBVxzOpgXLE7-bZWsav6we5T40g6eBk3Mc1nFPPSU130_provenance.
- NP78788.RA8rCBVxzOpgXLE7-bZWsav6we5T40g6eBk3Mc1nFPPSU130_assertion wasDerivedFrom gad-20150221 NP78788.RA8rCBVxzOpgXLE7-bZWsav6we5T40g6eBk3Mc1nFPPSU130_provenance.
- NP78788.RA8rCBVxzOpgXLE7-bZWsav6we5T40g6eBk3Mc1nFPPSU130_assertion SIO_000772 20851114 NP78788.RA8rCBVxzOpgXLE7-bZWsav6we5T40g6eBk3Mc1nFPPSU130_provenance.
- NP78788.RA8rCBVxzOpgXLE7-bZWsav6we5T40g6eBk3Mc1nFPPSU130_assertion evidence source_evidence_literature NP78788.RA8rCBVxzOpgXLE7-bZWsav6we5T40g6eBk3Mc1nFPPSU130_provenance.
- NP78788.RA8rCBVxzOpgXLE7-bZWsav6we5T40g6eBk3Mc1nFPPSU130_assertion description "[This HRM/sequencing procedure represents an inexpensive, highly sensitive and high-throughput method to allow identification of mutations in the coding sequences of prevalent LQTS genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78788.RA8rCBVxzOpgXLE7-bZWsav6we5T40g6eBk3Mc1nFPPSU130_provenance.