Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1313552.RAP-sGmAZD2jRCiNHfWkA0twa-fn-pIbTxbtbxTkIZatA130_provenance.