Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3641.RAw71ozgRRtIKh-aJJkSro1SE55rKNaDzyWiKJPRtbuA4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP3641.RAw71ozgRRtIKh-aJJkSro1SE55rKNaDzyWiKJPRtbuA4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3641.RAw71ozgRRtIKh-aJJkSro1SE55rKNaDzyWiKJPRtbuA4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3641.RAw71ozgRRtIKh-aJJkSro1SE55rKNaDzyWiKJPRtbuA4130_provenance.
- NP3641.RAw71ozgRRtIKh-aJJkSro1SE55rKNaDzyWiKJPRtbuA4130_assertion description "[Mutations in the gene encoding 3 beta-hydroxysteroid-delta 8, delta 7-isomerase cause X-linked dominant Conradi-HA1/4nermann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3641.RAw71ozgRRtIKh-aJJkSro1SE55rKNaDzyWiKJPRtbuA4130_provenance.
- NP3641.RAw71ozgRRtIKh-aJJkSro1SE55rKNaDzyWiKJPRtbuA4130_assertion evidence source_evidence_curated NP3641.RAw71ozgRRtIKh-aJJkSro1SE55rKNaDzyWiKJPRtbuA4130_provenance.
- NP3641.RAw71ozgRRtIKh-aJJkSro1SE55rKNaDzyWiKJPRtbuA4130_assertion SIO_000772 10391219 NP3641.RAw71ozgRRtIKh-aJJkSro1SE55rKNaDzyWiKJPRtbuA4130_provenance.
- NP3641.RAw71ozgRRtIKh-aJJkSro1SE55rKNaDzyWiKJPRtbuA4130_assertion wasDerivedFrom uniprot-20150221 NP3641.RAw71ozgRRtIKh-aJJkSro1SE55rKNaDzyWiKJPRtbuA4130_provenance.
- NP3641.RAw71ozgRRtIKh-aJJkSro1SE55rKNaDzyWiKJPRtbuA4130_assertion wasGeneratedBy ECO_0000218 NP3641.RAw71ozgRRtIKh-aJJkSro1SE55rKNaDzyWiKJPRtbuA4130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP3641.RAw71ozgRRtIKh-aJJkSro1SE55rKNaDzyWiKJPRtbuA4130_provenance.