Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP798647.RAfhhM6yxWwX3v40rPq4LdM1D4ZVMHVOA4LNkULtbZxKM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP798647.RAfhhM6yxWwX3v40rPq4LdM1D4ZVMHVOA4LNkULtbZxKM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP798647.RAfhhM6yxWwX3v40rPq4LdM1D4ZVMHVOA4LNkULtbZxKM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP798647.RAfhhM6yxWwX3v40rPq4LdM1D4ZVMHVOA4LNkULtbZxKM130_provenance.
- NP798647.RAfhhM6yxWwX3v40rPq4LdM1D4ZVMHVOA4LNkULtbZxKM130_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." NP798647.RAfhhM6yxWwX3v40rPq4LdM1D4ZVMHVOA4LNkULtbZxKM130_provenance.
- NP798647.RAfhhM6yxWwX3v40rPq4LdM1D4ZVMHVOA4LNkULtbZxKM130_assertion evidence source_evidence_literature NP798647.RAfhhM6yxWwX3v40rPq4LdM1D4ZVMHVOA4LNkULtbZxKM130_provenance.
- NP798647.RAfhhM6yxWwX3v40rPq4LdM1D4ZVMHVOA4LNkULtbZxKM130_assertion SIO_000772 20213484 NP798647.RAfhhM6yxWwX3v40rPq4LdM1D4ZVMHVOA4LNkULtbZxKM130_provenance.
- NP798647.RAfhhM6yxWwX3v40rPq4LdM1D4ZVMHVOA4LNkULtbZxKM130_assertion wasDerivedFrom befree-2016 NP798647.RAfhhM6yxWwX3v40rPq4LdM1D4ZVMHVOA4LNkULtbZxKM130_provenance.
- NP798647.RAfhhM6yxWwX3v40rPq4LdM1D4ZVMHVOA4LNkULtbZxKM130_assertion wasGeneratedBy ECO_0000203 NP798647.RAfhhM6yxWwX3v40rPq4LdM1D4ZVMHVOA4LNkULtbZxKM130_provenance.
- befree-2016 importedOn "2016-02-19" NP798647.RAfhhM6yxWwX3v40rPq4LdM1D4ZVMHVOA4LNkULtbZxKM130_provenance.