Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP917633.RAiY7-IyNe0HI5U4W90jAiRkP4yl3fRNtRaInPU0EWPYA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP917633.RAiY7-IyNe0HI5U4W90jAiRkP4yl3fRNtRaInPU0EWPYA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP917633.RAiY7-IyNe0HI5U4W90jAiRkP4yl3fRNtRaInPU0EWPYA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP917633.RAiY7-IyNe0HI5U4W90jAiRkP4yl3fRNtRaInPU0EWPYA130_provenance.
- NP917633.RAiY7-IyNe0HI5U4W90jAiRkP4yl3fRNtRaInPU0EWPYA130_assertion description "[The hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome is an autosomal dominant disorder caused by mutations of a member of the GATA-binding family of transcription factors, GATA3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917633.RAiY7-IyNe0HI5U4W90jAiRkP4yl3fRNtRaInPU0EWPYA130_provenance.
- NP917633.RAiY7-IyNe0HI5U4W90jAiRkP4yl3fRNtRaInPU0EWPYA130_assertion evidence source_evidence_literature NP917633.RAiY7-IyNe0HI5U4W90jAiRkP4yl3fRNtRaInPU0EWPYA130_provenance.
- NP917633.RAiY7-IyNe0HI5U4W90jAiRkP4yl3fRNtRaInPU0EWPYA130_assertion SIO_000772 15705923 NP917633.RAiY7-IyNe0HI5U4W90jAiRkP4yl3fRNtRaInPU0EWPYA130_provenance.
- NP917633.RAiY7-IyNe0HI5U4W90jAiRkP4yl3fRNtRaInPU0EWPYA130_assertion wasDerivedFrom befree-20150227 NP917633.RAiY7-IyNe0HI5U4W90jAiRkP4yl3fRNtRaInPU0EWPYA130_provenance.
- NP917633.RAiY7-IyNe0HI5U4W90jAiRkP4yl3fRNtRaInPU0EWPYA130_assertion wasGeneratedBy ECO_0000203 NP917633.RAiY7-IyNe0HI5U4W90jAiRkP4yl3fRNtRaInPU0EWPYA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP917633.RAiY7-IyNe0HI5U4W90jAiRkP4yl3fRNtRaInPU0EWPYA130_provenance.