Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP820056.RAqQHX9iUyWHC7bCoLu62PoGT4L8LwWVqHB1EywEsK5wo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP820056.RAqQHX9iUyWHC7bCoLu62PoGT4L8LwWVqHB1EywEsK5wo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP820056.RAqQHX9iUyWHC7bCoLu62PoGT4L8LwWVqHB1EywEsK5wo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP820056.RAqQHX9iUyWHC7bCoLu62PoGT4L8LwWVqHB1EywEsK5wo130_provenance.
- NP820056.RAqQHX9iUyWHC7bCoLu62PoGT4L8LwWVqHB1EywEsK5wo130_assertion description "[The ABCB1 3435 T allele and the ABCB1 2667 T-3435 T haplotype carriers were more frequent among subjects without extrapyramidal syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP820056.RAqQHX9iUyWHC7bCoLu62PoGT4L8LwWVqHB1EywEsK5wo130_provenance.
- NP820056.RAqQHX9iUyWHC7bCoLu62PoGT4L8LwWVqHB1EywEsK5wo130_assertion evidence source_evidence_literature NP820056.RAqQHX9iUyWHC7bCoLu62PoGT4L8LwWVqHB1EywEsK5wo130_provenance.
- NP820056.RAqQHX9iUyWHC7bCoLu62PoGT4L8LwWVqHB1EywEsK5wo130_assertion SIO_000772 20563569 NP820056.RAqQHX9iUyWHC7bCoLu62PoGT4L8LwWVqHB1EywEsK5wo130_provenance.
- NP820056.RAqQHX9iUyWHC7bCoLu62PoGT4L8LwWVqHB1EywEsK5wo130_assertion wasDerivedFrom befree-2016 NP820056.RAqQHX9iUyWHC7bCoLu62PoGT4L8LwWVqHB1EywEsK5wo130_provenance.
- NP820056.RAqQHX9iUyWHC7bCoLu62PoGT4L8LwWVqHB1EywEsK5wo130_assertion wasGeneratedBy ECO_0000203 NP820056.RAqQHX9iUyWHC7bCoLu62PoGT4L8LwWVqHB1EywEsK5wo130_provenance.
- befree-2016 importedOn "2016-02-19" NP820056.RAqQHX9iUyWHC7bCoLu62PoGT4L8LwWVqHB1EywEsK5wo130_provenance.