Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1332211.RA4RuYBqUuGw-cGjRP1GTs5Rl_Q2GDnzJYlpu_nEvs18A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1332211.RA4RuYBqUuGw-cGjRP1GTs5Rl_Q2GDnzJYlpu_nEvs18A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1332211.RA4RuYBqUuGw-cGjRP1GTs5Rl_Q2GDnzJYlpu_nEvs18A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1332211.RA4RuYBqUuGw-cGjRP1GTs5Rl_Q2GDnzJYlpu_nEvs18A130_provenance.
- NP1332211.RA4RuYBqUuGw-cGjRP1GTs5Rl_Q2GDnzJYlpu_nEvs18A130_assertion description "[Complete androgen insensitivity syndrome associated with a de novo mutation of the androgen receptor gene detected by single strand conformation polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1332211.RA4RuYBqUuGw-cGjRP1GTs5Rl_Q2GDnzJYlpu_nEvs18A130_provenance.
- NP1332211.RA4RuYBqUuGw-cGjRP1GTs5Rl_Q2GDnzJYlpu_nEvs18A130_assertion evidence source_evidence_literature NP1332211.RA4RuYBqUuGw-cGjRP1GTs5Rl_Q2GDnzJYlpu_nEvs18A130_provenance.
- NP1332211.RA4RuYBqUuGw-cGjRP1GTs5Rl_Q2GDnzJYlpu_nEvs18A130_assertion SIO_000772 8096390 NP1332211.RA4RuYBqUuGw-cGjRP1GTs5Rl_Q2GDnzJYlpu_nEvs18A130_provenance.
- NP1332211.RA4RuYBqUuGw-cGjRP1GTs5Rl_Q2GDnzJYlpu_nEvs18A130_assertion wasDerivedFrom befree-2016 NP1332211.RA4RuYBqUuGw-cGjRP1GTs5Rl_Q2GDnzJYlpu_nEvs18A130_provenance.
- NP1332211.RA4RuYBqUuGw-cGjRP1GTs5Rl_Q2GDnzJYlpu_nEvs18A130_assertion wasGeneratedBy ECO_0000203 NP1332211.RA4RuYBqUuGw-cGjRP1GTs5Rl_Q2GDnzJYlpu_nEvs18A130_provenance.
- befree-2016 importedOn "2016-02-19" NP1332211.RA4RuYBqUuGw-cGjRP1GTs5Rl_Q2GDnzJYlpu_nEvs18A130_provenance.