Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_assertion> ?p ?o ?g. }
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- NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_assertion type Assertion NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_head.
- NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_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." NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_provenance.
- NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_assertion evidence source_evidence_literature NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_provenance.
- NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_assertion SIO_000772 16078663 NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_provenance.
- NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_assertion wasDerivedFrom gad-20150221 NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_provenance.
- NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_assertion wasGeneratedBy ECO_0000203 NP94624.RAIepk8JyVx9y6wBOhteoNxBV6FsmGGZUfzIFqk3g-Gnw130_provenance.