Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP254031.RAPGAt1wuyTuB-MmspAKs2wxN_84xq-vF2XEMnLuVs-oU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP254031.RAPGAt1wuyTuB-MmspAKs2wxN_84xq-vF2XEMnLuVs-oU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP254031.RAPGAt1wuyTuB-MmspAKs2wxN_84xq-vF2XEMnLuVs-oU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP254031.RAPGAt1wuyTuB-MmspAKs2wxN_84xq-vF2XEMnLuVs-oU130_provenance.
- NP254031.RAPGAt1wuyTuB-MmspAKs2wxN_84xq-vF2XEMnLuVs-oU130_assertion description "[First, a Finnish study observed that the NAT2 slow acetylator phenotype was associated with an increased risk of MM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP254031.RAPGAt1wuyTuB-MmspAKs2wxN_84xq-vF2XEMnLuVs-oU130_provenance.
- NP254031.RAPGAt1wuyTuB-MmspAKs2wxN_84xq-vF2XEMnLuVs-oU130_assertion evidence source_evidence_literature NP254031.RAPGAt1wuyTuB-MmspAKs2wxN_84xq-vF2XEMnLuVs-oU130_provenance.
- NP254031.RAPGAt1wuyTuB-MmspAKs2wxN_84xq-vF2XEMnLuVs-oU130_assertion SIO_000772 18838334 NP254031.RAPGAt1wuyTuB-MmspAKs2wxN_84xq-vF2XEMnLuVs-oU130_provenance.
- NP254031.RAPGAt1wuyTuB-MmspAKs2wxN_84xq-vF2XEMnLuVs-oU130_assertion wasDerivedFrom befree-20140225 NP254031.RAPGAt1wuyTuB-MmspAKs2wxN_84xq-vF2XEMnLuVs-oU130_provenance.
- NP254031.RAPGAt1wuyTuB-MmspAKs2wxN_84xq-vF2XEMnLuVs-oU130_assertion wasGeneratedBy ECO_0000203 NP254031.RAPGAt1wuyTuB-MmspAKs2wxN_84xq-vF2XEMnLuVs-oU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP254031.RAPGAt1wuyTuB-MmspAKs2wxN_84xq-vF2XEMnLuVs-oU130_provenance.