Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP617985.RA75Jb8-1w0m8-aa_EHnq0uyDzNQSWPFBIC2fsPwsF4Ck130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP617985.RA75Jb8-1w0m8-aa_EHnq0uyDzNQSWPFBIC2fsPwsF4Ck130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP617985.RA75Jb8-1w0m8-aa_EHnq0uyDzNQSWPFBIC2fsPwsF4Ck130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP617985.RA75Jb8-1w0m8-aa_EHnq0uyDzNQSWPFBIC2fsPwsF4Ck130_provenance.
- NP617985.RA75Jb8-1w0m8-aa_EHnq0uyDzNQSWPFBIC2fsPwsF4Ck130_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." NP617985.RA75Jb8-1w0m8-aa_EHnq0uyDzNQSWPFBIC2fsPwsF4Ck130_provenance.
- NP617985.RA75Jb8-1w0m8-aa_EHnq0uyDzNQSWPFBIC2fsPwsF4Ck130_assertion evidence source_evidence_literature NP617985.RA75Jb8-1w0m8-aa_EHnq0uyDzNQSWPFBIC2fsPwsF4Ck130_provenance.
- NP617985.RA75Jb8-1w0m8-aa_EHnq0uyDzNQSWPFBIC2fsPwsF4Ck130_assertion SIO_000772 20563569 NP617985.RA75Jb8-1w0m8-aa_EHnq0uyDzNQSWPFBIC2fsPwsF4Ck130_provenance.
- NP617985.RA75Jb8-1w0m8-aa_EHnq0uyDzNQSWPFBIC2fsPwsF4Ck130_assertion wasDerivedFrom befree-20150227 NP617985.RA75Jb8-1w0m8-aa_EHnq0uyDzNQSWPFBIC2fsPwsF4Ck130_provenance.
- NP617985.RA75Jb8-1w0m8-aa_EHnq0uyDzNQSWPFBIC2fsPwsF4Ck130_assertion wasGeneratedBy ECO_0000203 NP617985.RA75Jb8-1w0m8-aa_EHnq0uyDzNQSWPFBIC2fsPwsF4Ck130_provenance.
- befree-20150227 importedOn "2015-02-27" NP617985.RA75Jb8-1w0m8-aa_EHnq0uyDzNQSWPFBIC2fsPwsF4Ck130_provenance.