Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP763886.RAgDETOIya8X6RN2IdnRNBMtDwo_2Y0_p1HY_A7lKi-Co130_assertion> ?p ?o ?g. }
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- NP763886.RAgDETOIya8X6RN2IdnRNBMtDwo_2Y0_p1HY_A7lKi-Co130_assertion type Assertion NP763886.RAgDETOIya8X6RN2IdnRNBMtDwo_2Y0_p1HY_A7lKi-Co130_head.
- NP763886.RAgDETOIya8X6RN2IdnRNBMtDwo_2Y0_p1HY_A7lKi-Co130_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." NP763886.RAgDETOIya8X6RN2IdnRNBMtDwo_2Y0_p1HY_A7lKi-Co130_provenance.
- NP763886.RAgDETOIya8X6RN2IdnRNBMtDwo_2Y0_p1HY_A7lKi-Co130_assertion evidence source_evidence_literature NP763886.RAgDETOIya8X6RN2IdnRNBMtDwo_2Y0_p1HY_A7lKi-Co130_provenance.
- NP763886.RAgDETOIya8X6RN2IdnRNBMtDwo_2Y0_p1HY_A7lKi-Co130_assertion SIO_000772 7901025 NP763886.RAgDETOIya8X6RN2IdnRNBMtDwo_2Y0_p1HY_A7lKi-Co130_provenance.
- NP763886.RAgDETOIya8X6RN2IdnRNBMtDwo_2Y0_p1HY_A7lKi-Co130_assertion wasDerivedFrom befree-20140225 NP763886.RAgDETOIya8X6RN2IdnRNBMtDwo_2Y0_p1HY_A7lKi-Co130_provenance.
- NP763886.RAgDETOIya8X6RN2IdnRNBMtDwo_2Y0_p1HY_A7lKi-Co130_assertion wasGeneratedBy ECO_0000203 NP763886.RAgDETOIya8X6RN2IdnRNBMtDwo_2Y0_p1HY_A7lKi-Co130_provenance.