Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP313299.RAv0k2o01S8QM4fE6wKi45Te7OG5QyENTm2OUzZljOzLo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP313299.RAv0k2o01S8QM4fE6wKi45Te7OG5QyENTm2OUzZljOzLo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP313299.RAv0k2o01S8QM4fE6wKi45Te7OG5QyENTm2OUzZljOzLo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP313299.RAv0k2o01S8QM4fE6wKi45Te7OG5QyENTm2OUzZljOzLo130_provenance.
- NP313299.RAv0k2o01S8QM4fE6wKi45Te7OG5QyENTm2OUzZljOzLo130_assertion description "[Frequent constitutional C to T mutations in CGA-arginine codons in the RB1 gene produce premature stop codons in patients with bilateral (hereditary) retinoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP313299.RAv0k2o01S8QM4fE6wKi45Te7OG5QyENTm2OUzZljOzLo130_provenance.
- NP313299.RAv0k2o01S8QM4fE6wKi45Te7OG5QyENTm2OUzZljOzLo130_assertion evidence source_evidence_literature NP313299.RAv0k2o01S8QM4fE6wKi45Te7OG5QyENTm2OUzZljOzLo130_provenance.
- NP313299.RAv0k2o01S8QM4fE6wKi45Te7OG5QyENTm2OUzZljOzLo130_assertion SIO_000772 7704558 NP313299.RAv0k2o01S8QM4fE6wKi45Te7OG5QyENTm2OUzZljOzLo130_provenance.
- NP313299.RAv0k2o01S8QM4fE6wKi45Te7OG5QyENTm2OUzZljOzLo130_assertion wasDerivedFrom befree-20150227 NP313299.RAv0k2o01S8QM4fE6wKi45Te7OG5QyENTm2OUzZljOzLo130_provenance.
- NP313299.RAv0k2o01S8QM4fE6wKi45Te7OG5QyENTm2OUzZljOzLo130_assertion wasGeneratedBy ECO_0000203 NP313299.RAv0k2o01S8QM4fE6wKi45Te7OG5QyENTm2OUzZljOzLo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP313299.RAv0k2o01S8QM4fE6wKi45Te7OG5QyENTm2OUzZljOzLo130_provenance.