Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP193097.RA6Ly32yBiGpV7eHGClQ4ngYVjqah6K0h_1z3v3NaoBZo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP193097.RA6Ly32yBiGpV7eHGClQ4ngYVjqah6K0h_1z3v3NaoBZo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193097.RA6Ly32yBiGpV7eHGClQ4ngYVjqah6K0h_1z3v3NaoBZo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193097.RA6Ly32yBiGpV7eHGClQ4ngYVjqah6K0h_1z3v3NaoBZo130_provenance.
- NP193097.RA6Ly32yBiGpV7eHGClQ4ngYVjqah6K0h_1z3v3NaoBZo130_assertion description "[We observed a somatic mutation in an FCD(IIb), i.e., amino-acid exchange at nucleotide position 834 (PTEN cDNA, GenBank AH007803.1) in exon 8 with replacement of phenylalanine by leucine (F278L).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193097.RA6Ly32yBiGpV7eHGClQ4ngYVjqah6K0h_1z3v3NaoBZo130_provenance.
- NP193097.RA6Ly32yBiGpV7eHGClQ4ngYVjqah6K0h_1z3v3NaoBZo130_assertion evidence source_evidence_literature NP193097.RA6Ly32yBiGpV7eHGClQ4ngYVjqah6K0h_1z3v3NaoBZo130_provenance.
- NP193097.RA6Ly32yBiGpV7eHGClQ4ngYVjqah6K0h_1z3v3NaoBZo130_assertion SIO_000772 17013611 NP193097.RA6Ly32yBiGpV7eHGClQ4ngYVjqah6K0h_1z3v3NaoBZo130_provenance.
- NP193097.RA6Ly32yBiGpV7eHGClQ4ngYVjqah6K0h_1z3v3NaoBZo130_assertion wasDerivedFrom befree-20140225 NP193097.RA6Ly32yBiGpV7eHGClQ4ngYVjqah6K0h_1z3v3NaoBZo130_provenance.
- NP193097.RA6Ly32yBiGpV7eHGClQ4ngYVjqah6K0h_1z3v3NaoBZo130_assertion wasGeneratedBy ECO_0000203 NP193097.RA6Ly32yBiGpV7eHGClQ4ngYVjqah6K0h_1z3v3NaoBZo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP193097.RA6Ly32yBiGpV7eHGClQ4ngYVjqah6K0h_1z3v3NaoBZo130_provenance.