Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1016895.RAhQuA0XG6N-6ZMGV-5GU3dS2FO2958BiVC9fgc1_o52Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1016895.RAhQuA0XG6N-6ZMGV-5GU3dS2FO2958BiVC9fgc1_o52Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1016895.RAhQuA0XG6N-6ZMGV-5GU3dS2FO2958BiVC9fgc1_o52Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1016895.RAhQuA0XG6N-6ZMGV-5GU3dS2FO2958BiVC9fgc1_o52Q130_provenance.
- NP1016895.RAhQuA0XG6N-6ZMGV-5GU3dS2FO2958BiVC9fgc1_o52Q130_assertion description "[Microdeletions in Yq11 are a common molecular cause of spermatogenic failure in men and are recurrently detected in about 10-15% of idiopathic azoospermia and severe oligozoospermia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1016895.RAhQuA0XG6N-6ZMGV-5GU3dS2FO2958BiVC9fgc1_o52Q130_provenance.
- NP1016895.RAhQuA0XG6N-6ZMGV-5GU3dS2FO2958BiVC9fgc1_o52Q130_assertion evidence source_evidence_literature NP1016895.RAhQuA0XG6N-6ZMGV-5GU3dS2FO2958BiVC9fgc1_o52Q130_provenance.
- NP1016895.RAhQuA0XG6N-6ZMGV-5GU3dS2FO2958BiVC9fgc1_o52Q130_assertion SIO_000772 16574598 NP1016895.RAhQuA0XG6N-6ZMGV-5GU3dS2FO2958BiVC9fgc1_o52Q130_provenance.
- NP1016895.RAhQuA0XG6N-6ZMGV-5GU3dS2FO2958BiVC9fgc1_o52Q130_assertion wasDerivedFrom befree-20150227 NP1016895.RAhQuA0XG6N-6ZMGV-5GU3dS2FO2958BiVC9fgc1_o52Q130_provenance.
- NP1016895.RAhQuA0XG6N-6ZMGV-5GU3dS2FO2958BiVC9fgc1_o52Q130_assertion wasGeneratedBy ECO_0000203 NP1016895.RAhQuA0XG6N-6ZMGV-5GU3dS2FO2958BiVC9fgc1_o52Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1016895.RAhQuA0XG6N-6ZMGV-5GU3dS2FO2958BiVC9fgc1_o52Q130_provenance.