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- source_evidence_literature type ECO_0000212 NP517140.RAacPsmZd2OOXJiqRV05acuSWBR5J2wS-TPnAuy_yJ8O0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP517140.RAacPsmZd2OOXJiqRV05acuSWBR5J2wS-TPnAuy_yJ8O0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP517140.RAacPsmZd2OOXJiqRV05acuSWBR5J2wS-TPnAuy_yJ8O0130_provenance.
- NP517140.RAacPsmZd2OOXJiqRV05acuSWBR5J2wS-TPnAuy_yJ8O0130_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." NP517140.RAacPsmZd2OOXJiqRV05acuSWBR5J2wS-TPnAuy_yJ8O0130_provenance.
- NP517140.RAacPsmZd2OOXJiqRV05acuSWBR5J2wS-TPnAuy_yJ8O0130_assertion evidence source_evidence_literature NP517140.RAacPsmZd2OOXJiqRV05acuSWBR5J2wS-TPnAuy_yJ8O0130_provenance.
- NP517140.RAacPsmZd2OOXJiqRV05acuSWBR5J2wS-TPnAuy_yJ8O0130_assertion SIO_000772 7901025 NP517140.RAacPsmZd2OOXJiqRV05acuSWBR5J2wS-TPnAuy_yJ8O0130_provenance.
- NP517140.RAacPsmZd2OOXJiqRV05acuSWBR5J2wS-TPnAuy_yJ8O0130_assertion wasDerivedFrom befree-20150227 NP517140.RAacPsmZd2OOXJiqRV05acuSWBR5J2wS-TPnAuy_yJ8O0130_provenance.
- NP517140.RAacPsmZd2OOXJiqRV05acuSWBR5J2wS-TPnAuy_yJ8O0130_assertion wasGeneratedBy ECO_0000203 NP517140.RAacPsmZd2OOXJiqRV05acuSWBR5J2wS-TPnAuy_yJ8O0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP517140.RAacPsmZd2OOXJiqRV05acuSWBR5J2wS-TPnAuy_yJ8O0130_provenance.