Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP699302.RAPcpDOH94ENse0Jeee2iC34w90pLtSeQbzsPbwSC0vdE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP699302.RAPcpDOH94ENse0Jeee2iC34w90pLtSeQbzsPbwSC0vdE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP699302.RAPcpDOH94ENse0Jeee2iC34w90pLtSeQbzsPbwSC0vdE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP699302.RAPcpDOH94ENse0Jeee2iC34w90pLtSeQbzsPbwSC0vdE130_provenance.
- NP699302.RAPcpDOH94ENse0Jeee2iC34w90pLtSeQbzsPbwSC0vdE130_assertion description "[To investigate whether defects in human PRDM9, CDK2 and PSMC3IP are associated with azoospermia Mutational analysis was performed in Japanese patients with azoospermia caused by meiotic arrest.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699302.RAPcpDOH94ENse0Jeee2iC34w90pLtSeQbzsPbwSC0vdE130_provenance.
- NP699302.RAPcpDOH94ENse0Jeee2iC34w90pLtSeQbzsPbwSC0vdE130_assertion evidence source_evidence_literature NP699302.RAPcpDOH94ENse0Jeee2iC34w90pLtSeQbzsPbwSC0vdE130_provenance.
- NP699302.RAPcpDOH94ENse0Jeee2iC34w90pLtSeQbzsPbwSC0vdE130_assertion SIO_000772 18941885 NP699302.RAPcpDOH94ENse0Jeee2iC34w90pLtSeQbzsPbwSC0vdE130_provenance.
- NP699302.RAPcpDOH94ENse0Jeee2iC34w90pLtSeQbzsPbwSC0vdE130_assertion wasDerivedFrom befree-2016 NP699302.RAPcpDOH94ENse0Jeee2iC34w90pLtSeQbzsPbwSC0vdE130_provenance.
- NP699302.RAPcpDOH94ENse0Jeee2iC34w90pLtSeQbzsPbwSC0vdE130_assertion wasGeneratedBy ECO_0000203 NP699302.RAPcpDOH94ENse0Jeee2iC34w90pLtSeQbzsPbwSC0vdE130_provenance.
- befree-2016 importedOn "2016-02-19" NP699302.RAPcpDOH94ENse0Jeee2iC34w90pLtSeQbzsPbwSC0vdE130_provenance.