Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP404875.RACALWy7DY2OKJJTnGxyK6XI5Bq3soGg52jDyiqPSlQ7k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP404875.RACALWy7DY2OKJJTnGxyK6XI5Bq3soGg52jDyiqPSlQ7k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404875.RACALWy7DY2OKJJTnGxyK6XI5Bq3soGg52jDyiqPSlQ7k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404875.RACALWy7DY2OKJJTnGxyK6XI5Bq3soGg52jDyiqPSlQ7k130_provenance.
- NP404875.RACALWy7DY2OKJJTnGxyK6XI5Bq3soGg52jDyiqPSlQ7k130_assertion description "[Mutations in 2 of these genes were shown to cause BFNC (KCNQ3) and hereditary deafness (KCNQ4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404875.RACALWy7DY2OKJJTnGxyK6XI5Bq3soGg52jDyiqPSlQ7k130_provenance.
- NP404875.RACALWy7DY2OKJJTnGxyK6XI5Bq3soGg52jDyiqPSlQ7k130_assertion evidence source_evidence_literature NP404875.RACALWy7DY2OKJJTnGxyK6XI5Bq3soGg52jDyiqPSlQ7k130_provenance.
- NP404875.RACALWy7DY2OKJJTnGxyK6XI5Bq3soGg52jDyiqPSlQ7k130_assertion SIO_000772 12707061 NP404875.RACALWy7DY2OKJJTnGxyK6XI5Bq3soGg52jDyiqPSlQ7k130_provenance.
- NP404875.RACALWy7DY2OKJJTnGxyK6XI5Bq3soGg52jDyiqPSlQ7k130_assertion wasDerivedFrom befree-20140225 NP404875.RACALWy7DY2OKJJTnGxyK6XI5Bq3soGg52jDyiqPSlQ7k130_provenance.
- NP404875.RACALWy7DY2OKJJTnGxyK6XI5Bq3soGg52jDyiqPSlQ7k130_assertion wasGeneratedBy ECO_0000203 NP404875.RACALWy7DY2OKJJTnGxyK6XI5Bq3soGg52jDyiqPSlQ7k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP404875.RACALWy7DY2OKJJTnGxyK6XI5Bq3soGg52jDyiqPSlQ7k130_provenance.