Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP286468.RAG-riBW3bBTOSRC2LBTogdVpbfcyEgzcXSDjh2Wv90vM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP286468.RAG-riBW3bBTOSRC2LBTogdVpbfcyEgzcXSDjh2Wv90vM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP286468.RAG-riBW3bBTOSRC2LBTogdVpbfcyEgzcXSDjh2Wv90vM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP286468.RAG-riBW3bBTOSRC2LBTogdVpbfcyEgzcXSDjh2Wv90vM130_provenance.
- befree-2016 importedOn "2016-02-19" NP286468.RAG-riBW3bBTOSRC2LBTogdVpbfcyEgzcXSDjh2Wv90vM130_provenance.
- NP286468.RAG-riBW3bBTOSRC2LBTogdVpbfcyEgzcXSDjh2Wv90vM130_assertion wasGeneratedBy ECO_0000203 NP286468.RAG-riBW3bBTOSRC2LBTogdVpbfcyEgzcXSDjh2Wv90vM130_provenance.
- NP286468.RAG-riBW3bBTOSRC2LBTogdVpbfcyEgzcXSDjh2Wv90vM130_assertion wasDerivedFrom befree-2016 NP286468.RAG-riBW3bBTOSRC2LBTogdVpbfcyEgzcXSDjh2Wv90vM130_provenance.
- NP286468.RAG-riBW3bBTOSRC2LBTogdVpbfcyEgzcXSDjh2Wv90vM130_assertion SIO_000772 10852552 NP286468.RAG-riBW3bBTOSRC2LBTogdVpbfcyEgzcXSDjh2Wv90vM130_provenance.
- NP286468.RAG-riBW3bBTOSRC2LBTogdVpbfcyEgzcXSDjh2Wv90vM130_assertion evidence source_evidence_literature NP286468.RAG-riBW3bBTOSRC2LBTogdVpbfcyEgzcXSDjh2Wv90vM130_provenance.
- NP286468.RAG-riBW3bBTOSRC2LBTogdVpbfcyEgzcXSDjh2Wv90vM130_assertion description "[A novel mutation of KCNQ3 (c.925T-->C) in a Japanese family with benign familial neonatal convulsions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP286468.RAG-riBW3bBTOSRC2LBTogdVpbfcyEgzcXSDjh2Wv90vM130_provenance.