Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP8177.RAOzqhf6pn0GBuSpCydxa_lgAXGIl-bUR3Rf495-PgWVA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8177.RAOzqhf6pn0GBuSpCydxa_lgAXGIl-bUR3Rf495-PgWVA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8177.RAOzqhf6pn0GBuSpCydxa_lgAXGIl-bUR3Rf495-PgWVA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8177.RAOzqhf6pn0GBuSpCydxa_lgAXGIl-bUR3Rf495-PgWVA130_provenance.
- NP8177.RAOzqhf6pn0GBuSpCydxa_lgAXGIl-bUR3Rf495-PgWVA130_assertion description "[Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8177.RAOzqhf6pn0GBuSpCydxa_lgAXGIl-bUR3Rf495-PgWVA130_provenance.
- NP8177.RAOzqhf6pn0GBuSpCydxa_lgAXGIl-bUR3Rf495-PgWVA130_assertion evidence source_evidence_curated NP8177.RAOzqhf6pn0GBuSpCydxa_lgAXGIl-bUR3Rf495-PgWVA130_provenance.
- NP8177.RAOzqhf6pn0GBuSpCydxa_lgAXGIl-bUR3Rf495-PgWVA130_assertion SIO_000772 19043416 NP8177.RAOzqhf6pn0GBuSpCydxa_lgAXGIl-bUR3Rf495-PgWVA130_provenance.
- NP8177.RAOzqhf6pn0GBuSpCydxa_lgAXGIl-bUR3Rf495-PgWVA130_assertion wasDerivedFrom ctd_human-20130708 NP8177.RAOzqhf6pn0GBuSpCydxa_lgAXGIl-bUR3Rf495-PgWVA130_provenance.
- NP8177.RAOzqhf6pn0GBuSpCydxa_lgAXGIl-bUR3Rf495-PgWVA130_assertion wasGeneratedBy ECO_0000218 NP8177.RAOzqhf6pn0GBuSpCydxa_lgAXGIl-bUR3Rf495-PgWVA130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP8177.RAOzqhf6pn0GBuSpCydxa_lgAXGIl-bUR3Rf495-PgWVA130_provenance.