Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_provenance.