Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP835506.RAjv8BaRjzPLJIC-_3uVsOhQWnBwUlf46wdU-ZBXSQWwM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP835506.RAjv8BaRjzPLJIC-_3uVsOhQWnBwUlf46wdU-ZBXSQWwM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835506.RAjv8BaRjzPLJIC-_3uVsOhQWnBwUlf46wdU-ZBXSQWwM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835506.RAjv8BaRjzPLJIC-_3uVsOhQWnBwUlf46wdU-ZBXSQWwM130_provenance.
- NP835506.RAjv8BaRjzPLJIC-_3uVsOhQWnBwUlf46wdU-ZBXSQWwM130_assertion description "[ARX mutations cause a diverse spectrum of human disorders, ranging from severe brain and genital malformations to non-syndromic intellectual disability (ID).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835506.RAjv8BaRjzPLJIC-_3uVsOhQWnBwUlf46wdU-ZBXSQWwM130_provenance.
- NP835506.RAjv8BaRjzPLJIC-_3uVsOhQWnBwUlf46wdU-ZBXSQWwM130_assertion evidence source_evidence_literature NP835506.RAjv8BaRjzPLJIC-_3uVsOhQWnBwUlf46wdU-ZBXSQWwM130_provenance.
- NP835506.RAjv8BaRjzPLJIC-_3uVsOhQWnBwUlf46wdU-ZBXSQWwM130_assertion SIO_000772 21496008 NP835506.RAjv8BaRjzPLJIC-_3uVsOhQWnBwUlf46wdU-ZBXSQWwM130_provenance.
- NP835506.RAjv8BaRjzPLJIC-_3uVsOhQWnBwUlf46wdU-ZBXSQWwM130_assertion wasDerivedFrom befree-20150227 NP835506.RAjv8BaRjzPLJIC-_3uVsOhQWnBwUlf46wdU-ZBXSQWwM130_provenance.
- NP835506.RAjv8BaRjzPLJIC-_3uVsOhQWnBwUlf46wdU-ZBXSQWwM130_assertion wasGeneratedBy ECO_0000203 NP835506.RAjv8BaRjzPLJIC-_3uVsOhQWnBwUlf46wdU-ZBXSQWwM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP835506.RAjv8BaRjzPLJIC-_3uVsOhQWnBwUlf46wdU-ZBXSQWwM130_provenance.