Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP237535.RAZ_rYsWQPcbP5bsJdH2IgROMpuPrKk6hW8IubwqhI0V0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP237535.RAZ_rYsWQPcbP5bsJdH2IgROMpuPrKk6hW8IubwqhI0V0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP237535.RAZ_rYsWQPcbP5bsJdH2IgROMpuPrKk6hW8IubwqhI0V0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP237535.RAZ_rYsWQPcbP5bsJdH2IgROMpuPrKk6hW8IubwqhI0V0130_provenance.
- NP237535.RAZ_rYsWQPcbP5bsJdH2IgROMpuPrKk6hW8IubwqhI0V0130_assertion description "[New mutation of the androgen receptor gene, as a deletion in exon 1 not described previously, was identified in a case of complete androgen insensitivity syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237535.RAZ_rYsWQPcbP5bsJdH2IgROMpuPrKk6hW8IubwqhI0V0130_provenance.
- NP237535.RAZ_rYsWQPcbP5bsJdH2IgROMpuPrKk6hW8IubwqhI0V0130_assertion evidence source_evidence_literature NP237535.RAZ_rYsWQPcbP5bsJdH2IgROMpuPrKk6hW8IubwqhI0V0130_provenance.
- NP237535.RAZ_rYsWQPcbP5bsJdH2IgROMpuPrKk6hW8IubwqhI0V0130_assertion SIO_000772 18462702 NP237535.RAZ_rYsWQPcbP5bsJdH2IgROMpuPrKk6hW8IubwqhI0V0130_provenance.
- NP237535.RAZ_rYsWQPcbP5bsJdH2IgROMpuPrKk6hW8IubwqhI0V0130_assertion wasDerivedFrom lhgdn-20090331 NP237535.RAZ_rYsWQPcbP5bsJdH2IgROMpuPrKk6hW8IubwqhI0V0130_provenance.
- NP237535.RAZ_rYsWQPcbP5bsJdH2IgROMpuPrKk6hW8IubwqhI0V0130_assertion wasGeneratedBy ECO_0000203 NP237535.RAZ_rYsWQPcbP5bsJdH2IgROMpuPrKk6hW8IubwqhI0V0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP237535.RAZ_rYsWQPcbP5bsJdH2IgROMpuPrKk6hW8IubwqhI0V0130_provenance.