Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP420058.RAdwkccu7tegJMFE6JDaklqPcoItrzB2JCqWldEr9DlFU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP420058.RAdwkccu7tegJMFE6JDaklqPcoItrzB2JCqWldEr9DlFU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420058.RAdwkccu7tegJMFE6JDaklqPcoItrzB2JCqWldEr9DlFU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420058.RAdwkccu7tegJMFE6JDaklqPcoItrzB2JCqWldEr9DlFU130_provenance.
- NP420058.RAdwkccu7tegJMFE6JDaklqPcoItrzB2JCqWldEr9DlFU130_assertion description "[The 208delG mutation in the FSCN2 gene produces not only autosomal dominant retinitis pigmentosa but also ADMD in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420058.RAdwkccu7tegJMFE6JDaklqPcoItrzB2JCqWldEr9DlFU130_provenance.
- NP420058.RAdwkccu7tegJMFE6JDaklqPcoItrzB2JCqWldEr9DlFU130_assertion evidence source_evidence_literature NP420058.RAdwkccu7tegJMFE6JDaklqPcoItrzB2JCqWldEr9DlFU130_provenance.
- NP420058.RAdwkccu7tegJMFE6JDaklqPcoItrzB2JCqWldEr9DlFU130_assertion SIO_000772 14609921 NP420058.RAdwkccu7tegJMFE6JDaklqPcoItrzB2JCqWldEr9DlFU130_provenance.
- NP420058.RAdwkccu7tegJMFE6JDaklqPcoItrzB2JCqWldEr9DlFU130_assertion wasDerivedFrom befree-2016 NP420058.RAdwkccu7tegJMFE6JDaklqPcoItrzB2JCqWldEr9DlFU130_provenance.
- NP420058.RAdwkccu7tegJMFE6JDaklqPcoItrzB2JCqWldEr9DlFU130_assertion wasGeneratedBy ECO_0000203 NP420058.RAdwkccu7tegJMFE6JDaklqPcoItrzB2JCqWldEr9DlFU130_provenance.
- befree-2016 importedOn "2016-02-19" NP420058.RAdwkccu7tegJMFE6JDaklqPcoItrzB2JCqWldEr9DlFU130_provenance.