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- source_evidence_literature type ECO_0000212 NP868052.RAIsQLXeRpbai_XeGm-4hlu2AhwrBp208zmw2KCGxRuZg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868052.RAIsQLXeRpbai_XeGm-4hlu2AhwrBp208zmw2KCGxRuZg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868052.RAIsQLXeRpbai_XeGm-4hlu2AhwrBp208zmw2KCGxRuZg130_provenance.
- NP868052.RAIsQLXeRpbai_XeGm-4hlu2AhwrBp208zmw2KCGxRuZg130_assertion description "[We found a lower gene and protein expression of CYP2R1 in samples with hypospermatogenesis and Sertoli-cell-only syndrome (P < 0.05) and a colocalization with INSL-3, a Leydig cell marker, at immunofluorescence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868052.RAIsQLXeRpbai_XeGm-4hlu2AhwrBp208zmw2KCGxRuZg130_provenance.
- NP868052.RAIsQLXeRpbai_XeGm-4hlu2AhwrBp208zmw2KCGxRuZg130_assertion evidence source_evidence_literature NP868052.RAIsQLXeRpbai_XeGm-4hlu2AhwrBp208zmw2KCGxRuZg130_provenance.
- NP868052.RAIsQLXeRpbai_XeGm-4hlu2AhwrBp208zmw2KCGxRuZg130_assertion SIO_000772 21270327 NP868052.RAIsQLXeRpbai_XeGm-4hlu2AhwrBp208zmw2KCGxRuZg130_provenance.
- NP868052.RAIsQLXeRpbai_XeGm-4hlu2AhwrBp208zmw2KCGxRuZg130_assertion wasDerivedFrom befree-2016 NP868052.RAIsQLXeRpbai_XeGm-4hlu2AhwrBp208zmw2KCGxRuZg130_provenance.
- NP868052.RAIsQLXeRpbai_XeGm-4hlu2AhwrBp208zmw2KCGxRuZg130_assertion wasGeneratedBy ECO_0000203 NP868052.RAIsQLXeRpbai_XeGm-4hlu2AhwrBp208zmw2KCGxRuZg130_provenance.
- befree-2016 importedOn "2016-02-19" NP868052.RAIsQLXeRpbai_XeGm-4hlu2AhwrBp208zmw2KCGxRuZg130_provenance.