Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP879505.RACZTYmeTuMarh_pCNE7AGvTdqX71dmLFtHQ143isSLoc130_assertion> ?p ?o ?g. }
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- NP879505.RACZTYmeTuMarh_pCNE7AGvTdqX71dmLFtHQ143isSLoc130_assertion type Assertion NP879505.RACZTYmeTuMarh_pCNE7AGvTdqX71dmLFtHQ143isSLoc130_head.
- NP879505.RACZTYmeTuMarh_pCNE7AGvTdqX71dmLFtHQ143isSLoc130_assertion wasGeneratedBy ECO_0000203 NP879505.RACZTYmeTuMarh_pCNE7AGvTdqX71dmLFtHQ143isSLoc130_provenance.
- NP879505.RACZTYmeTuMarh_pCNE7AGvTdqX71dmLFtHQ143isSLoc130_assertion wasDerivedFrom befree-2016 NP879505.RACZTYmeTuMarh_pCNE7AGvTdqX71dmLFtHQ143isSLoc130_provenance.
- NP879505.RACZTYmeTuMarh_pCNE7AGvTdqX71dmLFtHQ143isSLoc130_assertion SIO_000772 21403659 NP879505.RACZTYmeTuMarh_pCNE7AGvTdqX71dmLFtHQ143isSLoc130_provenance.
- NP879505.RACZTYmeTuMarh_pCNE7AGvTdqX71dmLFtHQ143isSLoc130_assertion evidence source_evidence_literature NP879505.RACZTYmeTuMarh_pCNE7AGvTdqX71dmLFtHQ143isSLoc130_provenance.
- NP879505.RACZTYmeTuMarh_pCNE7AGvTdqX71dmLFtHQ143isSLoc130_assertion description "[Although some cases of isolated cryptorchidism in humans can be ascribed to known genetic defects, such as mutations in INSL3 or RXFP2, the cause of cryptorchidism remains unknown in most patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP879505.RACZTYmeTuMarh_pCNE7AGvTdqX71dmLFtHQ143isSLoc130_provenance.