Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP254937.RAB0GNjTSykOMHdtgmDDpH4UIWTcH1GKP8HAHM3GRxGXk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP254937.RAB0GNjTSykOMHdtgmDDpH4UIWTcH1GKP8HAHM3GRxGXk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP254937.RAB0GNjTSykOMHdtgmDDpH4UIWTcH1GKP8HAHM3GRxGXk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP254937.RAB0GNjTSykOMHdtgmDDpH4UIWTcH1GKP8HAHM3GRxGXk130_provenance.
- NP254937.RAB0GNjTSykOMHdtgmDDpH4UIWTcH1GKP8HAHM3GRxGXk130_assertion description "[Polymorphisms in the LOXL1 gene confer risk to XFS/XFG in the Japanese, but there are different risk-associated alleles and haplotypes in the Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP254937.RAB0GNjTSykOMHdtgmDDpH4UIWTcH1GKP8HAHM3GRxGXk130_provenance.
- NP254937.RAB0GNjTSykOMHdtgmDDpH4UIWTcH1GKP8HAHM3GRxGXk130_assertion evidence source_evidence_literature NP254937.RAB0GNjTSykOMHdtgmDDpH4UIWTcH1GKP8HAHM3GRxGXk130_provenance.
- NP254937.RAB0GNjTSykOMHdtgmDDpH4UIWTcH1GKP8HAHM3GRxGXk130_assertion SIO_000772 18450598 NP254937.RAB0GNjTSykOMHdtgmDDpH4UIWTcH1GKP8HAHM3GRxGXk130_provenance.
- NP254937.RAB0GNjTSykOMHdtgmDDpH4UIWTcH1GKP8HAHM3GRxGXk130_assertion wasDerivedFrom befree-20140225 NP254937.RAB0GNjTSykOMHdtgmDDpH4UIWTcH1GKP8HAHM3GRxGXk130_provenance.
- NP254937.RAB0GNjTSykOMHdtgmDDpH4UIWTcH1GKP8HAHM3GRxGXk130_assertion wasGeneratedBy ECO_0000203 NP254937.RAB0GNjTSykOMHdtgmDDpH4UIWTcH1GKP8HAHM3GRxGXk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP254937.RAB0GNjTSykOMHdtgmDDpH4UIWTcH1GKP8HAHM3GRxGXk130_provenance.