Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP391388.RA4naQR1TAyPnqEur78SCj8VTBO0AtKX7uvOJpdtplibY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP391388.RA4naQR1TAyPnqEur78SCj8VTBO0AtKX7uvOJpdtplibY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP391388.RA4naQR1TAyPnqEur78SCj8VTBO0AtKX7uvOJpdtplibY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP391388.RA4naQR1TAyPnqEur78SCj8VTBO0AtKX7uvOJpdtplibY130_provenance.
- NP391388.RA4naQR1TAyPnqEur78SCj8VTBO0AtKX7uvOJpdtplibY130_assertion description "[A mutation in the 5'-UTR of IFITM5 creates an in-frame start codon and causes autosomal-dominant osteogenesis imperfecta type V with hyperplastic callus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391388.RA4naQR1TAyPnqEur78SCj8VTBO0AtKX7uvOJpdtplibY130_provenance.
- NP391388.RA4naQR1TAyPnqEur78SCj8VTBO0AtKX7uvOJpdtplibY130_assertion evidence source_evidence_literature NP391388.RA4naQR1TAyPnqEur78SCj8VTBO0AtKX7uvOJpdtplibY130_provenance.
- NP391388.RA4naQR1TAyPnqEur78SCj8VTBO0AtKX7uvOJpdtplibY130_assertion SIO_000772 22863195 NP391388.RA4naQR1TAyPnqEur78SCj8VTBO0AtKX7uvOJpdtplibY130_provenance.
- NP391388.RA4naQR1TAyPnqEur78SCj8VTBO0AtKX7uvOJpdtplibY130_assertion wasDerivedFrom befree-20140225 NP391388.RA4naQR1TAyPnqEur78SCj8VTBO0AtKX7uvOJpdtplibY130_provenance.
- NP391388.RA4naQR1TAyPnqEur78SCj8VTBO0AtKX7uvOJpdtplibY130_assertion wasGeneratedBy ECO_0000203 NP391388.RA4naQR1TAyPnqEur78SCj8VTBO0AtKX7uvOJpdtplibY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP391388.RA4naQR1TAyPnqEur78SCj8VTBO0AtKX7uvOJpdtplibY130_provenance.