Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP88875.RAHAn5d4FwSX5IGst5M24HtOasMEnvcTuUrcmJw5kuSpg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP88875.RAHAn5d4FwSX5IGst5M24HtOasMEnvcTuUrcmJw5kuSpg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP88875.RAHAn5d4FwSX5IGst5M24HtOasMEnvcTuUrcmJw5kuSpg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP88875.RAHAn5d4FwSX5IGst5M24HtOasMEnvcTuUrcmJw5kuSpg130_provenance.
- NP88875.RAHAn5d4FwSX5IGst5M24HtOasMEnvcTuUrcmJw5kuSpg130_assertion description "[A significant association with CM was found for the long allele of monoamine oxidase A 30 bp VNTR and CYP1A2*1F variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP88875.RAHAn5d4FwSX5IGst5M24HtOasMEnvcTuUrcmJw5kuSpg130_provenance.
- NP88875.RAHAn5d4FwSX5IGst5M24HtOasMEnvcTuUrcmJw5kuSpg130_assertion evidence source_evidence_literature NP88875.RAHAn5d4FwSX5IGst5M24HtOasMEnvcTuUrcmJw5kuSpg130_provenance.
- NP88875.RAHAn5d4FwSX5IGst5M24HtOasMEnvcTuUrcmJw5kuSpg130_assertion SIO_000772 20213484 NP88875.RAHAn5d4FwSX5IGst5M24HtOasMEnvcTuUrcmJw5kuSpg130_provenance.
- NP88875.RAHAn5d4FwSX5IGst5M24HtOasMEnvcTuUrcmJw5kuSpg130_assertion wasDerivedFrom gad-20130706 NP88875.RAHAn5d4FwSX5IGst5M24HtOasMEnvcTuUrcmJw5kuSpg130_provenance.
- NP88875.RAHAn5d4FwSX5IGst5M24HtOasMEnvcTuUrcmJw5kuSpg130_assertion wasGeneratedBy ECO_0000203 NP88875.RAHAn5d4FwSX5IGst5M24HtOasMEnvcTuUrcmJw5kuSpg130_provenance.
- gad-20130706 importedOn "2013-07-06" NP88875.RAHAn5d4FwSX5IGst5M24HtOasMEnvcTuUrcmJw5kuSpg130_provenance.