Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP399913.RA0Ja5xa_ctC9sSUHIYVS1D6A3KOgXnKHzIS-lKbmXhm4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP399913.RA0Ja5xa_ctC9sSUHIYVS1D6A3KOgXnKHzIS-lKbmXhm4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP399913.RA0Ja5xa_ctC9sSUHIYVS1D6A3KOgXnKHzIS-lKbmXhm4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP399913.RA0Ja5xa_ctC9sSUHIYVS1D6A3KOgXnKHzIS-lKbmXhm4130_provenance.
- NP399913.RA0Ja5xa_ctC9sSUHIYVS1D6A3KOgXnKHzIS-lKbmXhm4130_assertion description "[Autosomal-recessive and autosomal-dominant forms of WMS are caused by mutations in ADAMTS10 and FBN1 genes, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP399913.RA0Ja5xa_ctC9sSUHIYVS1D6A3KOgXnKHzIS-lKbmXhm4130_provenance.
- NP399913.RA0Ja5xa_ctC9sSUHIYVS1D6A3KOgXnKHzIS-lKbmXhm4130_assertion evidence source_evidence_literature NP399913.RA0Ja5xa_ctC9sSUHIYVS1D6A3KOgXnKHzIS-lKbmXhm4130_provenance.
- NP399913.RA0Ja5xa_ctC9sSUHIYVS1D6A3KOgXnKHzIS-lKbmXhm4130_assertion SIO_000772 19836009 NP399913.RA0Ja5xa_ctC9sSUHIYVS1D6A3KOgXnKHzIS-lKbmXhm4130_provenance.
- NP399913.RA0Ja5xa_ctC9sSUHIYVS1D6A3KOgXnKHzIS-lKbmXhm4130_assertion wasDerivedFrom befree-20140225 NP399913.RA0Ja5xa_ctC9sSUHIYVS1D6A3KOgXnKHzIS-lKbmXhm4130_provenance.
- NP399913.RA0Ja5xa_ctC9sSUHIYVS1D6A3KOgXnKHzIS-lKbmXhm4130_assertion wasGeneratedBy ECO_0000203 NP399913.RA0Ja5xa_ctC9sSUHIYVS1D6A3KOgXnKHzIS-lKbmXhm4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP399913.RA0Ja5xa_ctC9sSUHIYVS1D6A3KOgXnKHzIS-lKbmXhm4130_provenance.