Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_assertion> ?p ?o ?g. }
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- NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_assertion type Assertion NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_head.
- NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_assertion description "[In summary, missense mutations within the exons of the androgen receptor gene encoding the steroid-binding domain of the receptor are common causes of both partial and complete forms of androgen insensitivity syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_provenance.
- NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_assertion evidence source_evidence_literature NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_provenance.
- NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_assertion SIO_000772 7581399 NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_provenance.
- NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_assertion wasDerivedFrom befree-2016 NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_provenance.
- NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_assertion wasGeneratedBy ECO_0000203 NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_provenance.