Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP54641.RA1K3LCC32_CWlHY4AdVTjP-JYqidqJd4Swylz9TWJlvA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP54641.RA1K3LCC32_CWlHY4AdVTjP-JYqidqJd4Swylz9TWJlvA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP54641.RA1K3LCC32_CWlHY4AdVTjP-JYqidqJd4Swylz9TWJlvA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP54641.RA1K3LCC32_CWlHY4AdVTjP-JYqidqJd4Swylz9TWJlvA130_provenance.
- NP54641.RA1K3LCC32_CWlHY4AdVTjP-JYqidqJd4Swylz9TWJlvA130_assertion description "[There is a high frequency of chromosomal abnormality and DAZ gene copy deletion in patients with azoospermia and oligospermia, which suggests that chromosomal abnormality and partial and complete deletion of DAZ gene copy might be important genetic causes of Chinese male infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54641.RA1K3LCC32_CWlHY4AdVTjP-JYqidqJd4Swylz9TWJlvA130_provenance.
- NP54641.RA1K3LCC32_CWlHY4AdVTjP-JYqidqJd4Swylz9TWJlvA130_assertion evidence source_evidence_literature NP54641.RA1K3LCC32_CWlHY4AdVTjP-JYqidqJd4Swylz9TWJlvA130_provenance.
- NP54641.RA1K3LCC32_CWlHY4AdVTjP-JYqidqJd4Swylz9TWJlvA130_assertion SIO_000772 16078663 NP54641.RA1K3LCC32_CWlHY4AdVTjP-JYqidqJd4Swylz9TWJlvA130_provenance.
- NP54641.RA1K3LCC32_CWlHY4AdVTjP-JYqidqJd4Swylz9TWJlvA130_assertion wasDerivedFrom gad-20150221 NP54641.RA1K3LCC32_CWlHY4AdVTjP-JYqidqJd4Swylz9TWJlvA130_provenance.
- NP54641.RA1K3LCC32_CWlHY4AdVTjP-JYqidqJd4Swylz9TWJlvA130_assertion wasGeneratedBy ECO_0000203 NP54641.RA1K3LCC32_CWlHY4AdVTjP-JYqidqJd4Swylz9TWJlvA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP54641.RA1K3LCC32_CWlHY4AdVTjP-JYqidqJd4Swylz9TWJlvA130_provenance.