Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP413430.RAeuhvyrG50SsI6NdZZIJ3goWWG8GI_3O_htzXZJQEXRE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP413430.RAeuhvyrG50SsI6NdZZIJ3goWWG8GI_3O_htzXZJQEXRE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP413430.RAeuhvyrG50SsI6NdZZIJ3goWWG8GI_3O_htzXZJQEXRE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP413430.RAeuhvyrG50SsI6NdZZIJ3goWWG8GI_3O_htzXZJQEXRE130_provenance.
- NP413430.RAeuhvyrG50SsI6NdZZIJ3goWWG8GI_3O_htzXZJQEXRE130_assertion description "[Furthermore, NR5A1 mutations have now been found in women with familial and sporadic 46,XX primary ovarian insufficiency without adrenal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP413430.RAeuhvyrG50SsI6NdZZIJ3goWWG8GI_3O_htzXZJQEXRE130_provenance.
- NP413430.RAeuhvyrG50SsI6NdZZIJ3goWWG8GI_3O_htzXZJQEXRE130_assertion evidence source_evidence_literature NP413430.RAeuhvyrG50SsI6NdZZIJ3goWWG8GI_3O_htzXZJQEXRE130_provenance.
- NP413430.RAeuhvyrG50SsI6NdZZIJ3goWWG8GI_3O_htzXZJQEXRE130_assertion SIO_000772 20595937 NP413430.RAeuhvyrG50SsI6NdZZIJ3goWWG8GI_3O_htzXZJQEXRE130_provenance.
- NP413430.RAeuhvyrG50SsI6NdZZIJ3goWWG8GI_3O_htzXZJQEXRE130_assertion wasDerivedFrom befree-20150227 NP413430.RAeuhvyrG50SsI6NdZZIJ3goWWG8GI_3O_htzXZJQEXRE130_provenance.
- NP413430.RAeuhvyrG50SsI6NdZZIJ3goWWG8GI_3O_htzXZJQEXRE130_assertion wasGeneratedBy ECO_0000203 NP413430.RAeuhvyrG50SsI6NdZZIJ3goWWG8GI_3O_htzXZJQEXRE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP413430.RAeuhvyrG50SsI6NdZZIJ3goWWG8GI_3O_htzXZJQEXRE130_provenance.