Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP347041.RAa2iKXCGkfTdFWZMn6BMxZMFinj-UcJKu3vQ48ECqHvY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP347041.RAa2iKXCGkfTdFWZMn6BMxZMFinj-UcJKu3vQ48ECqHvY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP347041.RAa2iKXCGkfTdFWZMn6BMxZMFinj-UcJKu3vQ48ECqHvY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP347041.RAa2iKXCGkfTdFWZMn6BMxZMFinj-UcJKu3vQ48ECqHvY130_provenance.
- befree-2016 importedOn "2016-02-19" NP347041.RAa2iKXCGkfTdFWZMn6BMxZMFinj-UcJKu3vQ48ECqHvY130_provenance.
- NP347041.RAa2iKXCGkfTdFWZMn6BMxZMFinj-UcJKu3vQ48ECqHvY130_assertion wasGeneratedBy ECO_0000203 NP347041.RAa2iKXCGkfTdFWZMn6BMxZMFinj-UcJKu3vQ48ECqHvY130_provenance.
- NP347041.RAa2iKXCGkfTdFWZMn6BMxZMFinj-UcJKu3vQ48ECqHvY130_assertion wasDerivedFrom befree-2016 NP347041.RAa2iKXCGkfTdFWZMn6BMxZMFinj-UcJKu3vQ48ECqHvY130_provenance.
- NP347041.RAa2iKXCGkfTdFWZMn6BMxZMFinj-UcJKu3vQ48ECqHvY130_assertion SIO_000772 11875049 NP347041.RAa2iKXCGkfTdFWZMn6BMxZMFinj-UcJKu3vQ48ECqHvY130_provenance.
- NP347041.RAa2iKXCGkfTdFWZMn6BMxZMFinj-UcJKu3vQ48ECqHvY130_assertion evidence source_evidence_literature NP347041.RAa2iKXCGkfTdFWZMn6BMxZMFinj-UcJKu3vQ48ECqHvY130_provenance.
- NP347041.RAa2iKXCGkfTdFWZMn6BMxZMFinj-UcJKu3vQ48ECqHvY130_assertion description "[Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho(-/-) mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347041.RAa2iKXCGkfTdFWZMn6BMxZMFinj-UcJKu3vQ48ECqHvY130_provenance.