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- source_evidence_literature type ECO_0000212 NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_provenance.
- NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_assertion description "[Alpha-1 antitrypsin (?1AT) deficiency is a common autosomal recessive disorder characterized by a marked reduction in serum ?1AT levels, lung and liver disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_provenance.
- NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_assertion evidence source_evidence_literature NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_provenance.
- NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_assertion SIO_000772 24191907 NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_provenance.
- NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_assertion wasDerivedFrom befree-20150227 NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_provenance.
- NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_assertion wasGeneratedBy ECO_0000203 NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_provenance.