Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP989439.RA4JykVjIHPAs4FpspiHgLy-QCczh9Blx8mH4FEiQglsk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP989439.RA4JykVjIHPAs4FpspiHgLy-QCczh9Blx8mH4FEiQglsk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP989439.RA4JykVjIHPAs4FpspiHgLy-QCczh9Blx8mH4FEiQglsk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP989439.RA4JykVjIHPAs4FpspiHgLy-QCczh9Blx8mH4FEiQglsk130_provenance.
- NP989439.RA4JykVjIHPAs4FpspiHgLy-QCczh9Blx8mH4FEiQglsk130_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." NP989439.RA4JykVjIHPAs4FpspiHgLy-QCczh9Blx8mH4FEiQglsk130_provenance.
- NP989439.RA4JykVjIHPAs4FpspiHgLy-QCczh9Blx8mH4FEiQglsk130_assertion evidence source_evidence_literature NP989439.RA4JykVjIHPAs4FpspiHgLy-QCczh9Blx8mH4FEiQglsk130_provenance.
- NP989439.RA4JykVjIHPAs4FpspiHgLy-QCczh9Blx8mH4FEiQglsk130_assertion SIO_000772 22863195 NP989439.RA4JykVjIHPAs4FpspiHgLy-QCczh9Blx8mH4FEiQglsk130_provenance.
- NP989439.RA4JykVjIHPAs4FpspiHgLy-QCczh9Blx8mH4FEiQglsk130_assertion wasDerivedFrom befree-20150227 NP989439.RA4JykVjIHPAs4FpspiHgLy-QCczh9Blx8mH4FEiQglsk130_provenance.
- NP989439.RA4JykVjIHPAs4FpspiHgLy-QCczh9Blx8mH4FEiQglsk130_assertion wasGeneratedBy ECO_0000203 NP989439.RA4JykVjIHPAs4FpspiHgLy-QCczh9Blx8mH4FEiQglsk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP989439.RA4JykVjIHPAs4FpspiHgLy-QCczh9Blx8mH4FEiQglsk130_provenance.