Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP83072.RAMpRqQvNoJyI8-ozNnyS9ik4o4jUuSPOyJmvCUTu_Cao130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP83072.RAMpRqQvNoJyI8-ozNnyS9ik4o4jUuSPOyJmvCUTu_Cao130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP83072.RAMpRqQvNoJyI8-ozNnyS9ik4o4jUuSPOyJmvCUTu_Cao130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP83072.RAMpRqQvNoJyI8-ozNnyS9ik4o4jUuSPOyJmvCUTu_Cao130_provenance.
- NP83072.RAMpRqQvNoJyI8-ozNnyS9ik4o4jUuSPOyJmvCUTu_Cao130_assertion description "[Our study provides the first demonstration of the association of the polymorphism of the MHC2TA gene with genetic risk for AAD that appears to be independent from the well-known association with the polymorphism of HLA class II genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83072.RAMpRqQvNoJyI8-ozNnyS9ik4o4jUuSPOyJmvCUTu_Cao130_provenance.
- NP83072.RAMpRqQvNoJyI8-ozNnyS9ik4o4jUuSPOyJmvCUTu_Cao130_assertion evidence source_evidence_literature NP83072.RAMpRqQvNoJyI8-ozNnyS9ik4o4jUuSPOyJmvCUTu_Cao130_provenance.
- NP83072.RAMpRqQvNoJyI8-ozNnyS9ik4o4jUuSPOyJmvCUTu_Cao130_assertion SIO_000772 16849401 NP83072.RAMpRqQvNoJyI8-ozNnyS9ik4o4jUuSPOyJmvCUTu_Cao130_provenance.
- NP83072.RAMpRqQvNoJyI8-ozNnyS9ik4o4jUuSPOyJmvCUTu_Cao130_assertion wasDerivedFrom gad-20150221 NP83072.RAMpRqQvNoJyI8-ozNnyS9ik4o4jUuSPOyJmvCUTu_Cao130_provenance.
- NP83072.RAMpRqQvNoJyI8-ozNnyS9ik4o4jUuSPOyJmvCUTu_Cao130_assertion wasGeneratedBy ECO_0000203 NP83072.RAMpRqQvNoJyI8-ozNnyS9ik4o4jUuSPOyJmvCUTu_Cao130_provenance.
- gad-20150221 importedOn "2015-02-21" NP83072.RAMpRqQvNoJyI8-ozNnyS9ik4o4jUuSPOyJmvCUTu_Cao130_provenance.