Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_assertion type Assertion NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_head.
- NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_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." NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_provenance.
- NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_assertion evidence source_evidence_literature NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_provenance.
- NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_assertion SIO_000772 23319530 NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_provenance.
- NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_assertion wasDerivedFrom befree-20150227 NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_provenance.
- NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_assertion wasGeneratedBy ECO_0000203 NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_provenance.