Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP480883.RA6UuDz47AOeSLVk2nQxRf8MSATiPsgBDh_2lQ6ZJ_URA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP480883.RA6UuDz47AOeSLVk2nQxRf8MSATiPsgBDh_2lQ6ZJ_URA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP480883.RA6UuDz47AOeSLVk2nQxRf8MSATiPsgBDh_2lQ6ZJ_URA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP480883.RA6UuDz47AOeSLVk2nQxRf8MSATiPsgBDh_2lQ6ZJ_URA130_provenance.
- NP480883.RA6UuDz47AOeSLVk2nQxRf8MSATiPsgBDh_2lQ6ZJ_URA130_assertion description "[Interestingly, both patients displayed multifocal osteomyelitis, which is often seen in patients with Mendelian susceptibility to mycobacterial diseases with autosomal dominant partial IFN-?R1 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480883.RA6UuDz47AOeSLVk2nQxRf8MSATiPsgBDh_2lQ6ZJ_URA130_provenance.
- NP480883.RA6UuDz47AOeSLVk2nQxRf8MSATiPsgBDh_2lQ6ZJ_URA130_assertion evidence source_evidence_literature NP480883.RA6UuDz47AOeSLVk2nQxRf8MSATiPsgBDh_2lQ6ZJ_URA130_provenance.
- NP480883.RA6UuDz47AOeSLVk2nQxRf8MSATiPsgBDh_2lQ6ZJ_URA130_assertion SIO_000772 23585529 NP480883.RA6UuDz47AOeSLVk2nQxRf8MSATiPsgBDh_2lQ6ZJ_URA130_provenance.
- NP480883.RA6UuDz47AOeSLVk2nQxRf8MSATiPsgBDh_2lQ6ZJ_URA130_assertion wasDerivedFrom befree-20150227 NP480883.RA6UuDz47AOeSLVk2nQxRf8MSATiPsgBDh_2lQ6ZJ_URA130_provenance.
- NP480883.RA6UuDz47AOeSLVk2nQxRf8MSATiPsgBDh_2lQ6ZJ_URA130_assertion wasGeneratedBy ECO_0000203 NP480883.RA6UuDz47AOeSLVk2nQxRf8MSATiPsgBDh_2lQ6ZJ_URA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP480883.RA6UuDz47AOeSLVk2nQxRf8MSATiPsgBDh_2lQ6ZJ_URA130_provenance.