Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP874174.RALIFQ_YKQizdNYXe1Qv9inwmBavdGEsW_Zm0esLkhvXA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP874174.RALIFQ_YKQizdNYXe1Qv9inwmBavdGEsW_Zm0esLkhvXA130_assertion type Assertion NP874174.RALIFQ_YKQizdNYXe1Qv9inwmBavdGEsW_Zm0esLkhvXA130_head.
- NP874174.RALIFQ_YKQizdNYXe1Qv9inwmBavdGEsW_Zm0esLkhvXA130_assertion description "[However, mutations in SRY are not frequent especially in cases of 46,XY partial gonadal dysgenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874174.RALIFQ_YKQizdNYXe1Qv9inwmBavdGEsW_Zm0esLkhvXA130_provenance.
- NP874174.RALIFQ_YKQizdNYXe1Qv9inwmBavdGEsW_Zm0esLkhvXA130_assertion evidence source_evidence_literature NP874174.RALIFQ_YKQizdNYXe1Qv9inwmBavdGEsW_Zm0esLkhvXA130_provenance.
- NP874174.RALIFQ_YKQizdNYXe1Qv9inwmBavdGEsW_Zm0esLkhvXA130_assertion SIO_000772 21340164 NP874174.RALIFQ_YKQizdNYXe1Qv9inwmBavdGEsW_Zm0esLkhvXA130_provenance.
- NP874174.RALIFQ_YKQizdNYXe1Qv9inwmBavdGEsW_Zm0esLkhvXA130_assertion wasDerivedFrom befree-2016 NP874174.RALIFQ_YKQizdNYXe1Qv9inwmBavdGEsW_Zm0esLkhvXA130_provenance.
- NP874174.RALIFQ_YKQizdNYXe1Qv9inwmBavdGEsW_Zm0esLkhvXA130_assertion wasGeneratedBy ECO_0000203 NP874174.RALIFQ_YKQizdNYXe1Qv9inwmBavdGEsW_Zm0esLkhvXA130_provenance.