Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP329109.RAPBTsiKXvM5MUPI47JJNyJqbEOi0rbROJxJvnqo9jgNM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP329109.RAPBTsiKXvM5MUPI47JJNyJqbEOi0rbROJxJvnqo9jgNM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP329109.RAPBTsiKXvM5MUPI47JJNyJqbEOi0rbROJxJvnqo9jgNM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP329109.RAPBTsiKXvM5MUPI47JJNyJqbEOi0rbROJxJvnqo9jgNM130_provenance.
- NP329109.RAPBTsiKXvM5MUPI47JJNyJqbEOi0rbROJxJvnqo9jgNM130_assertion description "[The CFTR gene mutations or IVS8-5T variant in at least 1 allele was identified with similar frequencies among the AZOO (33%) and CRYPTO (21%) patients; 55% of the AZOO patients with normal spermatogenesis (NS) had mutations in 1 or 2 alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329109.RAPBTsiKXvM5MUPI47JJNyJqbEOi0rbROJxJvnqo9jgNM130_provenance.
- NP329109.RAPBTsiKXvM5MUPI47JJNyJqbEOi0rbROJxJvnqo9jgNM130_assertion evidence source_evidence_literature NP329109.RAPBTsiKXvM5MUPI47JJNyJqbEOi0rbROJxJvnqo9jgNM130_provenance.
- NP329109.RAPBTsiKXvM5MUPI47JJNyJqbEOi0rbROJxJvnqo9jgNM130_assertion SIO_000772 16572913 NP329109.RAPBTsiKXvM5MUPI47JJNyJqbEOi0rbROJxJvnqo9jgNM130_provenance.
- NP329109.RAPBTsiKXvM5MUPI47JJNyJqbEOi0rbROJxJvnqo9jgNM130_assertion wasDerivedFrom befree-20140225 NP329109.RAPBTsiKXvM5MUPI47JJNyJqbEOi0rbROJxJvnqo9jgNM130_provenance.
- NP329109.RAPBTsiKXvM5MUPI47JJNyJqbEOi0rbROJxJvnqo9jgNM130_assertion wasGeneratedBy ECO_0000203 NP329109.RAPBTsiKXvM5MUPI47JJNyJqbEOi0rbROJxJvnqo9jgNM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP329109.RAPBTsiKXvM5MUPI47JJNyJqbEOi0rbROJxJvnqo9jgNM130_provenance.