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- source_evidence_literature type ECO_0000212 NP76155.RAcxJgP7AzwwN73r0_IOitH50lFGk3XxKdIJMrWwpAWLY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP76155.RAcxJgP7AzwwN73r0_IOitH50lFGk3XxKdIJMrWwpAWLY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP76155.RAcxJgP7AzwwN73r0_IOitH50lFGk3XxKdIJMrWwpAWLY130_provenance.
- NP76155.RAcxJgP7AzwwN73r0_IOitH50lFGk3XxKdIJMrWwpAWLY130_assertion description "[Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2, KCNQ1, and WFS1 in type 2 diabetes in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP76155.RAcxJgP7AzwwN73r0_IOitH50lFGk3XxKdIJMrWwpAWLY130_provenance.
- NP76155.RAcxJgP7AzwwN73r0_IOitH50lFGk3XxKdIJMrWwpAWLY130_assertion evidence source_evidence_literature NP76155.RAcxJgP7AzwwN73r0_IOitH50lFGk3XxKdIJMrWwpAWLY130_provenance.
- NP76155.RAcxJgP7AzwwN73r0_IOitH50lFGk3XxKdIJMrWwpAWLY130_assertion SIO_000772 20509872 NP76155.RAcxJgP7AzwwN73r0_IOitH50lFGk3XxKdIJMrWwpAWLY130_provenance.
- NP76155.RAcxJgP7AzwwN73r0_IOitH50lFGk3XxKdIJMrWwpAWLY130_assertion wasDerivedFrom gad-20150221 NP76155.RAcxJgP7AzwwN73r0_IOitH50lFGk3XxKdIJMrWwpAWLY130_provenance.
- NP76155.RAcxJgP7AzwwN73r0_IOitH50lFGk3XxKdIJMrWwpAWLY130_assertion wasGeneratedBy ECO_0000203 NP76155.RAcxJgP7AzwwN73r0_IOitH50lFGk3XxKdIJMrWwpAWLY130_provenance.
- gad-20150221 importedOn "2015-02-21" NP76155.RAcxJgP7AzwwN73r0_IOitH50lFGk3XxKdIJMrWwpAWLY130_provenance.