Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_provenance.
- NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_assertion description "[We found no strong evidence of association for any of these loci with AD in this population. While the possibility exists that the genes analysed are involved in AD (ie they have weak effects and/or are population specific), results reinforce the need for extensive replication studies if we are to be successful in defining true risk factors in complex diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_provenance.
- NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_assertion evidence source_evidence_literature NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_provenance.
- NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_assertion SIO_000772 11436125 NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_provenance.
- NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_assertion wasDerivedFrom gad-20130706 NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_provenance.
- NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_assertion wasGeneratedBy ECO_0000203 NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_provenance.
- gad-20130706 importedOn "2013-07-06" NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_provenance.