Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP329014.RANoKvj3w_YAvh2QNuI0FqJMr-0riESXJ0boDvWNMOUAc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP329014.RANoKvj3w_YAvh2QNuI0FqJMr-0riESXJ0boDvWNMOUAc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP329014.RANoKvj3w_YAvh2QNuI0FqJMr-0riESXJ0boDvWNMOUAc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP329014.RANoKvj3w_YAvh2QNuI0FqJMr-0riESXJ0boDvWNMOUAc130_provenance.
- NP329014.RANoKvj3w_YAvh2QNuI0FqJMr-0riESXJ0boDvWNMOUAc130_assertion description "[Diagnoses included Drash syndrome with Wilms tumor in infancy (3 patients), partial androgen insensitivity resulting from androgen receptor mutations (2), true hermaphroditism (2), chromosomal aberration (1), deficiency of antim�llerian hormone (1), gonadal dysgenesis (1), partial 5 alpha-reductase deficiency caused by a novel point mutation (1), and XX-male syndrome (1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329014.RANoKvj3w_YAvh2QNuI0FqJMr-0riESXJ0boDvWNMOUAc130_provenance.
- NP329014.RANoKvj3w_YAvh2QNuI0FqJMr-0riESXJ0boDvWNMOUAc130_assertion evidence source_evidence_literature NP329014.RANoKvj3w_YAvh2QNuI0FqJMr-0riESXJ0boDvWNMOUAc130_provenance.
- NP329014.RANoKvj3w_YAvh2QNuI0FqJMr-0riESXJ0boDvWNMOUAc130_assertion SIO_000772 9329414 NP329014.RANoKvj3w_YAvh2QNuI0FqJMr-0riESXJ0boDvWNMOUAc130_provenance.
- NP329014.RANoKvj3w_YAvh2QNuI0FqJMr-0riESXJ0boDvWNMOUAc130_assertion wasDerivedFrom befree-20140225 NP329014.RANoKvj3w_YAvh2QNuI0FqJMr-0riESXJ0boDvWNMOUAc130_provenance.
- NP329014.RANoKvj3w_YAvh2QNuI0FqJMr-0riESXJ0boDvWNMOUAc130_assertion wasGeneratedBy ECO_0000203 NP329014.RANoKvj3w_YAvh2QNuI0FqJMr-0riESXJ0boDvWNMOUAc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP329014.RANoKvj3w_YAvh2QNuI0FqJMr-0riESXJ0boDvWNMOUAc130_provenance.