Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1043887.RA98UMMKi-Lym4w3WsVJo2BQrr-f9y6Hpo8xxWjx79OrE130_assertion> ?p ?o ?g. }
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- NP1043887.RA98UMMKi-Lym4w3WsVJo2BQrr-f9y6Hpo8xxWjx79OrE130_assertion type Assertion NP1043887.RA98UMMKi-Lym4w3WsVJo2BQrr-f9y6Hpo8xxWjx79OrE130_head.
- NP1043887.RA98UMMKi-Lym4w3WsVJo2BQrr-f9y6Hpo8xxWjx79OrE130_assertion description "[Thus, the phenotype associated with the unique combination of mutations uncovered in both patients expands the spectrum of disease associated with TMPRSS6 mutations to include iron deficiency anemia that is accompanied by hyperferritinemia at initial presentation and is responsive to continued oral iron therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1043887.RA98UMMKi-Lym4w3WsVJo2BQrr-f9y6Hpo8xxWjx79OrE130_provenance.
- NP1043887.RA98UMMKi-Lym4w3WsVJo2BQrr-f9y6Hpo8xxWjx79OrE130_assertion evidence source_evidence_literature NP1043887.RA98UMMKi-Lym4w3WsVJo2BQrr-f9y6Hpo8xxWjx79OrE130_provenance.
- NP1043887.RA98UMMKi-Lym4w3WsVJo2BQrr-f9y6Hpo8xxWjx79OrE130_assertion SIO_000772 23319530 NP1043887.RA98UMMKi-Lym4w3WsVJo2BQrr-f9y6Hpo8xxWjx79OrE130_provenance.
- NP1043887.RA98UMMKi-Lym4w3WsVJo2BQrr-f9y6Hpo8xxWjx79OrE130_assertion wasDerivedFrom befree-2016 NP1043887.RA98UMMKi-Lym4w3WsVJo2BQrr-f9y6Hpo8xxWjx79OrE130_provenance.
- NP1043887.RA98UMMKi-Lym4w3WsVJo2BQrr-f9y6Hpo8xxWjx79OrE130_assertion wasGeneratedBy ECO_0000203 NP1043887.RA98UMMKi-Lym4w3WsVJo2BQrr-f9y6Hpo8xxWjx79OrE130_provenance.