Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP506405.RA0h9fKGT2_tkAQiwN75B7a2pBZMYicTr77zUXtWKNvq8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP506405.RA0h9fKGT2_tkAQiwN75B7a2pBZMYicTr77zUXtWKNvq8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP506405.RA0h9fKGT2_tkAQiwN75B7a2pBZMYicTr77zUXtWKNvq8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP506405.RA0h9fKGT2_tkAQiwN75B7a2pBZMYicTr77zUXtWKNvq8130_provenance.
- NP506405.RA0h9fKGT2_tkAQiwN75B7a2pBZMYicTr77zUXtWKNvq8130_assertion description "[We found that the GNB3 T allele produces a significant risk for AD in individuals homozygous for the ADRB1 C allele, suggesting that the combined effect of both polymorphisms influences AD susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP506405.RA0h9fKGT2_tkAQiwN75B7a2pBZMYicTr77zUXtWKNvq8130_provenance.
- NP506405.RA0h9fKGT2_tkAQiwN75B7a2pBZMYicTr77zUXtWKNvq8130_assertion evidence source_evidence_literature NP506405.RA0h9fKGT2_tkAQiwN75B7a2pBZMYicTr77zUXtWKNvq8130_provenance.
- NP506405.RA0h9fKGT2_tkAQiwN75B7a2pBZMYicTr77zUXtWKNvq8130_assertion SIO_000772 15212839 NP506405.RA0h9fKGT2_tkAQiwN75B7a2pBZMYicTr77zUXtWKNvq8130_provenance.
- NP506405.RA0h9fKGT2_tkAQiwN75B7a2pBZMYicTr77zUXtWKNvq8130_assertion wasDerivedFrom befree-20140225 NP506405.RA0h9fKGT2_tkAQiwN75B7a2pBZMYicTr77zUXtWKNvq8130_provenance.
- NP506405.RA0h9fKGT2_tkAQiwN75B7a2pBZMYicTr77zUXtWKNvq8130_assertion wasGeneratedBy ECO_0000203 NP506405.RA0h9fKGT2_tkAQiwN75B7a2pBZMYicTr77zUXtWKNvq8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP506405.RA0h9fKGT2_tkAQiwN75B7a2pBZMYicTr77zUXtWKNvq8130_provenance.