Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP15632.RABmr3sXD3G9RZkR9ovbtzuNQITvMfRfdnOl1U2hf8nnU130_assertion> ?p ?o ?g. }
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- NP15632.RABmr3sXD3G9RZkR9ovbtzuNQITvMfRfdnOl1U2hf8nnU130_assertion type Assertion NP15632.RABmr3sXD3G9RZkR9ovbtzuNQITvMfRfdnOl1U2hf8nnU130_head.
- NP15632.RABmr3sXD3G9RZkR9ovbtzuNQITvMfRfdnOl1U2hf8nnU130_assertion description "[Erythropoietic protoporphyria (EPP) is an inherited defect of the ferrochelatase (FECH) gene characterized by the accumulation of toxic protoporphyrin in the liver and bone marrow resulting in severe skin photosensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP15632.RABmr3sXD3G9RZkR9ovbtzuNQITvMfRfdnOl1U2hf8nnU130_provenance.
- NP15632.RABmr3sXD3G9RZkR9ovbtzuNQITvMfRfdnOl1U2hf8nnU130_assertion evidence source_evidence_curated NP15632.RABmr3sXD3G9RZkR9ovbtzuNQITvMfRfdnOl1U2hf8nnU130_provenance.
- NP15632.RABmr3sXD3G9RZkR9ovbtzuNQITvMfRfdnOl1U2hf8nnU130_assertion SIO_000772 15284838 NP15632.RABmr3sXD3G9RZkR9ovbtzuNQITvMfRfdnOl1U2hf8nnU130_provenance.
- NP15632.RABmr3sXD3G9RZkR9ovbtzuNQITvMfRfdnOl1U2hf8nnU130_assertion wasDerivedFrom ctd_human-20130708 NP15632.RABmr3sXD3G9RZkR9ovbtzuNQITvMfRfdnOl1U2hf8nnU130_provenance.
- NP15632.RABmr3sXD3G9RZkR9ovbtzuNQITvMfRfdnOl1U2hf8nnU130_assertion wasGeneratedBy ECO_0000218 NP15632.RABmr3sXD3G9RZkR9ovbtzuNQITvMfRfdnOl1U2hf8nnU130_provenance.