Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP576939.RABLIDKu7MbdozX5GIQm_6qr3R_3RyFV8kfE02Ir9okJI130_assertion> ?p ?o ?g. }
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- NP576939.RABLIDKu7MbdozX5GIQm_6qr3R_3RyFV8kfE02Ir9okJI130_assertion type Assertion NP576939.RABLIDKu7MbdozX5GIQm_6qr3R_3RyFV8kfE02Ir9okJI130_head.
- NP576939.RABLIDKu7MbdozX5GIQm_6qr3R_3RyFV8kfE02Ir9okJI130_assertion description "[We screened 1186 men from infertile couples for Y chromosome deletions, and identified three unrelated oligozoospermic men and one azoospermic man who carry an identical 768 kb deletion resulting in loss of the entire P4 palindrome, including both HSFY genes, the only coding genes within the deletion interval.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576939.RABLIDKu7MbdozX5GIQm_6qr3R_3RyFV8kfE02Ir9okJI130_provenance.
- NP576939.RABLIDKu7MbdozX5GIQm_6qr3R_3RyFV8kfE02Ir9okJI130_assertion evidence source_evidence_literature NP576939.RABLIDKu7MbdozX5GIQm_6qr3R_3RyFV8kfE02Ir9okJI130_provenance.
- NP576939.RABLIDKu7MbdozX5GIQm_6qr3R_3RyFV8kfE02Ir9okJI130_assertion SIO_000772 22158087 NP576939.RABLIDKu7MbdozX5GIQm_6qr3R_3RyFV8kfE02Ir9okJI130_provenance.
- NP576939.RABLIDKu7MbdozX5GIQm_6qr3R_3RyFV8kfE02Ir9okJI130_assertion wasDerivedFrom befree-20140225 NP576939.RABLIDKu7MbdozX5GIQm_6qr3R_3RyFV8kfE02Ir9okJI130_provenance.
- NP576939.RABLIDKu7MbdozX5GIQm_6qr3R_3RyFV8kfE02Ir9okJI130_assertion wasGeneratedBy ECO_0000203 NP576939.RABLIDKu7MbdozX5GIQm_6qr3R_3RyFV8kfE02Ir9okJI130_provenance.