Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP499171.RA0i8eNgYdMX9VC9u5I7LM8TnpouMXC6HV0XxxGxBba-M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP499171.RA0i8eNgYdMX9VC9u5I7LM8TnpouMXC6HV0XxxGxBba-M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499171.RA0i8eNgYdMX9VC9u5I7LM8TnpouMXC6HV0XxxGxBba-M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499171.RA0i8eNgYdMX9VC9u5I7LM8TnpouMXC6HV0XxxGxBba-M130_provenance.
- NP499171.RA0i8eNgYdMX9VC9u5I7LM8TnpouMXC6HV0XxxGxBba-M130_assertion description "[Mutation of acceptor splice site of the SEDL gene in X-linked spondyloepiphyseal dysplasia tarda causes the activation of cryptic splice site.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499171.RA0i8eNgYdMX9VC9u5I7LM8TnpouMXC6HV0XxxGxBba-M130_provenance.
- NP499171.RA0i8eNgYdMX9VC9u5I7LM8TnpouMXC6HV0XxxGxBba-M130_assertion evidence source_evidence_literature NP499171.RA0i8eNgYdMX9VC9u5I7LM8TnpouMXC6HV0XxxGxBba-M130_provenance.
- NP499171.RA0i8eNgYdMX9VC9u5I7LM8TnpouMXC6HV0XxxGxBba-M130_assertion SIO_000772 15952107 NP499171.RA0i8eNgYdMX9VC9u5I7LM8TnpouMXC6HV0XxxGxBba-M130_provenance.
- NP499171.RA0i8eNgYdMX9VC9u5I7LM8TnpouMXC6HV0XxxGxBba-M130_assertion wasDerivedFrom befree-2016 NP499171.RA0i8eNgYdMX9VC9u5I7LM8TnpouMXC6HV0XxxGxBba-M130_provenance.
- NP499171.RA0i8eNgYdMX9VC9u5I7LM8TnpouMXC6HV0XxxGxBba-M130_assertion wasGeneratedBy ECO_0000203 NP499171.RA0i8eNgYdMX9VC9u5I7LM8TnpouMXC6HV0XxxGxBba-M130_provenance.
- befree-2016 importedOn "2016-02-19" NP499171.RA0i8eNgYdMX9VC9u5I7LM8TnpouMXC6HV0XxxGxBba-M130_provenance.