Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP761348.RAbu67xAruXWu1DS_La8_5p1tn-RkI7-frV2ZuOZH4tbE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP761348.RAbu67xAruXWu1DS_La8_5p1tn-RkI7-frV2ZuOZH4tbE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP761348.RAbu67xAruXWu1DS_La8_5p1tn-RkI7-frV2ZuOZH4tbE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP761348.RAbu67xAruXWu1DS_La8_5p1tn-RkI7-frV2ZuOZH4tbE130_provenance.
- NP761348.RAbu67xAruXWu1DS_La8_5p1tn-RkI7-frV2ZuOZH4tbE130_assertion description "[Among the congenital sideroblastic anemias (CSAs), the most common form is X-linked sideroblastic anemia, due to mutations in 5-aminolevulinate synthase (ALAS2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761348.RAbu67xAruXWu1DS_La8_5p1tn-RkI7-frV2ZuOZH4tbE130_provenance.
- NP761348.RAbu67xAruXWu1DS_La8_5p1tn-RkI7-frV2ZuOZH4tbE130_assertion evidence source_evidence_literature NP761348.RAbu67xAruXWu1DS_La8_5p1tn-RkI7-frV2ZuOZH4tbE130_provenance.
- NP761348.RAbu67xAruXWu1DS_La8_5p1tn-RkI7-frV2ZuOZH4tbE130_assertion SIO_000772 19731322 NP761348.RAbu67xAruXWu1DS_La8_5p1tn-RkI7-frV2ZuOZH4tbE130_provenance.
- NP761348.RAbu67xAruXWu1DS_La8_5p1tn-RkI7-frV2ZuOZH4tbE130_assertion wasDerivedFrom befree-2016 NP761348.RAbu67xAruXWu1DS_La8_5p1tn-RkI7-frV2ZuOZH4tbE130_provenance.
- NP761348.RAbu67xAruXWu1DS_La8_5p1tn-RkI7-frV2ZuOZH4tbE130_assertion wasGeneratedBy ECO_0000203 NP761348.RAbu67xAruXWu1DS_La8_5p1tn-RkI7-frV2ZuOZH4tbE130_provenance.
- befree-2016 importedOn "2016-02-19" NP761348.RAbu67xAruXWu1DS_La8_5p1tn-RkI7-frV2ZuOZH4tbE130_provenance.