Matches in Nanopublications for { ?s ?p "[In humans, this could explain that low levels of hepcidin found during juvenile haemochromatosis and HFE-1 genetic haemochromatosis are associated with an iron overload phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 12 of
12
with 100 items per page.
- assertion description "[In humans, this could explain that low levels of hepcidin found during juvenile haemochromatosis and HFE-1 genetic haemochromatosis are associated with an iron overload phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP552568.RAGESGCAvO-FX04-ryl5N1NYDlEMmgnl1OOlRO9SOJyYE130_assertion description "[In humans, this could explain that low levels of hepcidin found during juvenile haemochromatosis and HFE-1 genetic haemochromatosis are associated with an iron overload phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552568.RAGESGCAvO-FX04-ryl5N1NYDlEMmgnl1OOlRO9SOJyYE130_provenance.
- assertion description "[In humans, this could explain that low levels of hepcidin found during juvenile haemochromatosis and HFE-1 genetic haemochromatosis are associated with an iron overload phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP500711.RACP4Em3WH9gWe0rNy1KIGlyUaIdCahAiw58vHAiswrVQ130_assertion description "[In humans, this could explain that low levels of hepcidin found during juvenile haemochromatosis and HFE-1 genetic haemochromatosis are associated with an iron overload phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500711.RACP4Em3WH9gWe0rNy1KIGlyUaIdCahAiw58vHAiswrVQ130_provenance.
- NP500712.RACZ67edNRO-DHIWsQw5ApLykvMe8HqJ_MKwvo-Mi2PfU130_assertion description "[In humans, this could explain that low levels of hepcidin found during juvenile haemochromatosis and HFE-1 genetic haemochromatosis are associated with an iron overload phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500712.RACZ67edNRO-DHIWsQw5ApLykvMe8HqJ_MKwvo-Mi2PfU130_provenance.
- NP500708.RAb6j-n8DL8zm6fvxDybFN1__3-a106UBkwL81erts5g0130_assertion description "[In humans, this could explain that low levels of hepcidin found during juvenile haemochromatosis and HFE-1 genetic haemochromatosis are associated with an iron overload phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500708.RAb6j-n8DL8zm6fvxDybFN1__3-a106UBkwL81erts5g0130_provenance.
- assertion description "[In humans, this could explain that low levels of hepcidin found during juvenile haemochromatosis and HFE-1 genetic haemochromatosis are associated with an iron overload phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[In humans, this could explain that low levels of hepcidin found during juvenile haemochromatosis and HFE-1 genetic haemochromatosis are associated with an iron overload phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP500706.RAoOru5SRovUb-8FnoI2gJr7too9DychBIoQcRYCULFoo130_assertion description "[In humans, this could explain that low levels of hepcidin found during juvenile haemochromatosis and HFE-1 genetic haemochromatosis are associated with an iron overload phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500706.RAoOru5SRovUb-8FnoI2gJr7too9DychBIoQcRYCULFoo130_provenance.
- NP500710.RAvNx6y2VTGhV_Q-6zajXaQ3EkVRmmkmEll2aqJvzbT1U130_assertion description "[In humans, this could explain that low levels of hepcidin found during juvenile haemochromatosis and HFE-1 genetic haemochromatosis are associated with an iron overload phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500710.RAvNx6y2VTGhV_Q-6zajXaQ3EkVRmmkmEll2aqJvzbT1U130_provenance.
- NP447111.RA9GQppStqKzhmd14Of_owxyPulqn_ZC29d4u7Mh9R9LE130_assertion description "[In humans, this could explain that low levels of hepcidin found during juvenile haemochromatosis and HFE-1 genetic haemochromatosis are associated with an iron overload phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP447111.RA9GQppStqKzhmd14Of_owxyPulqn_ZC29d4u7Mh9R9LE130_provenance.
- NP500707.RA3DpFIIpNmv9BxulJwORB2yujoetpKBV8bMhfJHWX3iM130_assertion description "[In humans, this could explain that low levels of hepcidin found during juvenile haemochromatosis and HFE-1 genetic haemochromatosis are associated with an iron overload phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500707.RA3DpFIIpNmv9BxulJwORB2yujoetpKBV8bMhfJHWX3iM130_provenance.