Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP228486.RAjiN1OQE2JHgu5cXS4l-g6kM2v_x6gk055YY0w6eVMj8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP228486.RAjiN1OQE2JHgu5cXS4l-g6kM2v_x6gk055YY0w6eVMj8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP228486.RAjiN1OQE2JHgu5cXS4l-g6kM2v_x6gk055YY0w6eVMj8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP228486.RAjiN1OQE2JHgu5cXS4l-g6kM2v_x6gk055YY0w6eVMj8130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP228486.RAjiN1OQE2JHgu5cXS4l-g6kM2v_x6gk055YY0w6eVMj8130_provenance.
- NP228486.RAjiN1OQE2JHgu5cXS4l-g6kM2v_x6gk055YY0w6eVMj8130_assertion wasGeneratedBy ECO_0000203 NP228486.RAjiN1OQE2JHgu5cXS4l-g6kM2v_x6gk055YY0w6eVMj8130_provenance.
- NP228486.RAjiN1OQE2JHgu5cXS4l-g6kM2v_x6gk055YY0w6eVMj8130_assertion wasDerivedFrom lhgdn-20090331 NP228486.RAjiN1OQE2JHgu5cXS4l-g6kM2v_x6gk055YY0w6eVMj8130_provenance.
- NP228486.RAjiN1OQE2JHgu5cXS4l-g6kM2v_x6gk055YY0w6eVMj8130_assertion SIO_000772 17714709 NP228486.RAjiN1OQE2JHgu5cXS4l-g6kM2v_x6gk055YY0w6eVMj8130_provenance.
- NP228486.RAjiN1OQE2JHgu5cXS4l-g6kM2v_x6gk055YY0w6eVMj8130_assertion evidence source_evidence_literature NP228486.RAjiN1OQE2JHgu5cXS4l-g6kM2v_x6gk055YY0w6eVMj8130_provenance.
- NP228486.RAjiN1OQE2JHgu5cXS4l-g6kM2v_x6gk055YY0w6eVMj8130_assertion description "[Androgen receptor gene mutations located in the N-terminal transactivation domain, are a novel mutation c.118delA presumed to result in a complete loss of AR function and to be associated with complete androgen insensitivity syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP228486.RAjiN1OQE2JHgu5cXS4l-g6kM2v_x6gk055YY0w6eVMj8130_provenance.