Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP334081.RAnrZe5QyHcaSyRx8h4hPC1-_vo9J-C-MFrPJdAl9pChc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP334081.RAnrZe5QyHcaSyRx8h4hPC1-_vo9J-C-MFrPJdAl9pChc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP334081.RAnrZe5QyHcaSyRx8h4hPC1-_vo9J-C-MFrPJdAl9pChc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP334081.RAnrZe5QyHcaSyRx8h4hPC1-_vo9J-C-MFrPJdAl9pChc130_provenance.
- NP334081.RAnrZe5QyHcaSyRx8h4hPC1-_vo9J-C-MFrPJdAl9pChc130_assertion description "[Leukocyte adhesion deficiency type 1 (LAD I) is an autosomal recessive disorder caused by mutations in the ITGB2 gene, encoding the beta2 integrin family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP334081.RAnrZe5QyHcaSyRx8h4hPC1-_vo9J-C-MFrPJdAl9pChc130_provenance.
- NP334081.RAnrZe5QyHcaSyRx8h4hPC1-_vo9J-C-MFrPJdAl9pChc130_assertion evidence source_evidence_literature NP334081.RAnrZe5QyHcaSyRx8h4hPC1-_vo9J-C-MFrPJdAl9pChc130_provenance.
- NP334081.RAnrZe5QyHcaSyRx8h4hPC1-_vo9J-C-MFrPJdAl9pChc130_assertion SIO_000772 20549317 NP334081.RAnrZe5QyHcaSyRx8h4hPC1-_vo9J-C-MFrPJdAl9pChc130_provenance.
- NP334081.RAnrZe5QyHcaSyRx8h4hPC1-_vo9J-C-MFrPJdAl9pChc130_assertion wasDerivedFrom befree-20140225 NP334081.RAnrZe5QyHcaSyRx8h4hPC1-_vo9J-C-MFrPJdAl9pChc130_provenance.
- NP334081.RAnrZe5QyHcaSyRx8h4hPC1-_vo9J-C-MFrPJdAl9pChc130_assertion wasGeneratedBy ECO_0000203 NP334081.RAnrZe5QyHcaSyRx8h4hPC1-_vo9J-C-MFrPJdAl9pChc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP334081.RAnrZe5QyHcaSyRx8h4hPC1-_vo9J-C-MFrPJdAl9pChc130_provenance.