Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP707771.RAX9x_x6AIsF2oZpaxt9BOR3Y-JDCmlj09aPHxc8159JE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP707771.RAX9x_x6AIsF2oZpaxt9BOR3Y-JDCmlj09aPHxc8159JE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP707771.RAX9x_x6AIsF2oZpaxt9BOR3Y-JDCmlj09aPHxc8159JE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP707771.RAX9x_x6AIsF2oZpaxt9BOR3Y-JDCmlj09aPHxc8159JE130_provenance.
- NP707771.RAX9x_x6AIsF2oZpaxt9BOR3Y-JDCmlj09aPHxc8159JE130_assertion description "[Distinct rare missense mutations of the TP53 gene were detected in Capi1 (codon 312) and Capi3 (codon 181); the codon 181 mutation is consistent with a previously reported similar finding in a small series of CUP specimens.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP707771.RAX9x_x6AIsF2oZpaxt9BOR3Y-JDCmlj09aPHxc8159JE130_provenance.
- NP707771.RAX9x_x6AIsF2oZpaxt9BOR3Y-JDCmlj09aPHxc8159JE130_assertion evidence source_evidence_literature NP707771.RAX9x_x6AIsF2oZpaxt9BOR3Y-JDCmlj09aPHxc8159JE130_provenance.
- NP707771.RAX9x_x6AIsF2oZpaxt9BOR3Y-JDCmlj09aPHxc8159JE130_assertion SIO_000772 18088404 NP707771.RAX9x_x6AIsF2oZpaxt9BOR3Y-JDCmlj09aPHxc8159JE130_provenance.
- NP707771.RAX9x_x6AIsF2oZpaxt9BOR3Y-JDCmlj09aPHxc8159JE130_assertion wasDerivedFrom befree-20140225 NP707771.RAX9x_x6AIsF2oZpaxt9BOR3Y-JDCmlj09aPHxc8159JE130_provenance.
- NP707771.RAX9x_x6AIsF2oZpaxt9BOR3Y-JDCmlj09aPHxc8159JE130_assertion wasGeneratedBy ECO_0000203 NP707771.RAX9x_x6AIsF2oZpaxt9BOR3Y-JDCmlj09aPHxc8159JE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP707771.RAX9x_x6AIsF2oZpaxt9BOR3Y-JDCmlj09aPHxc8159JE130_provenance.