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- source_evidence_literature type ECO_0000212 NP1325433.RAAnrk5yr2bwa-BOOZ0qenc1oyvtCqCNmekQXKlNPueYQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1325433.RAAnrk5yr2bwa-BOOZ0qenc1oyvtCqCNmekQXKlNPueYQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1325433.RAAnrk5yr2bwa-BOOZ0qenc1oyvtCqCNmekQXKlNPueYQ130_provenance.
- NP1325433.RAAnrk5yr2bwa-BOOZ0qenc1oyvtCqCNmekQXKlNPueYQ130_assertion description "[Leukocyte adhesion deficiency (LAD) is an autosomal recessive disease caused by heterogeneous mutations within the gene encoding the common beta subunit (CD18) of the three leukocyte integrins LFA-1 (CD11a/CD18), Mac-1 (CD11b/CD18), and p150,95 (CD11c/CD18).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1325433.RAAnrk5yr2bwa-BOOZ0qenc1oyvtCqCNmekQXKlNPueYQ130_provenance.
- NP1325433.RAAnrk5yr2bwa-BOOZ0qenc1oyvtCqCNmekQXKlNPueYQ130_assertion evidence source_evidence_literature NP1325433.RAAnrk5yr2bwa-BOOZ0qenc1oyvtCqCNmekQXKlNPueYQ130_provenance.
- NP1325433.RAAnrk5yr2bwa-BOOZ0qenc1oyvtCqCNmekQXKlNPueYQ130_assertion SIO_000772 7901025 NP1325433.RAAnrk5yr2bwa-BOOZ0qenc1oyvtCqCNmekQXKlNPueYQ130_provenance.
- NP1325433.RAAnrk5yr2bwa-BOOZ0qenc1oyvtCqCNmekQXKlNPueYQ130_assertion wasDerivedFrom befree-2016 NP1325433.RAAnrk5yr2bwa-BOOZ0qenc1oyvtCqCNmekQXKlNPueYQ130_provenance.
- NP1325433.RAAnrk5yr2bwa-BOOZ0qenc1oyvtCqCNmekQXKlNPueYQ130_assertion wasGeneratedBy ECO_0000203 NP1325433.RAAnrk5yr2bwa-BOOZ0qenc1oyvtCqCNmekQXKlNPueYQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1325433.RAAnrk5yr2bwa-BOOZ0qenc1oyvtCqCNmekQXKlNPueYQ130_provenance.