Matches in Nanopublications for { ?s ?p "[Feline acute intermittent porphyria: a phenocopy masquerading as an erythropoietic porphyria due to dominant and recessive hydroxymethylbilane synthase mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 4 of
4
with 100 items per page.
- NP854013.RAVSTP0n1YotS4Ym0QDa4VX3SjzP5PPOaAHwM5xvMZp50130_assertion description "[Feline acute intermittent porphyria: a phenocopy masquerading as an erythropoietic porphyria due to dominant and recessive hydroxymethylbilane synthase mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854013.RAVSTP0n1YotS4Ym0QDa4VX3SjzP5PPOaAHwM5xvMZp50130_provenance.
- assertion description "[Feline acute intermittent porphyria: a phenocopy masquerading as an erythropoietic porphyria due to dominant and recessive hydroxymethylbilane synthase mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP182034.RANYPR0Op2wZdL8MWUm6aX3onayB6sFVnUjYf9SGwt5B0130_assertion description "[Feline acute intermittent porphyria: a phenocopy masquerading as an erythropoietic porphyria due to dominant and recessive hydroxymethylbilane synthase mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182034.RANYPR0Op2wZdL8MWUm6aX3onayB6sFVnUjYf9SGwt5B0130_provenance.
- assertion description "[Feline acute intermittent porphyria: a phenocopy masquerading as an erythropoietic porphyria due to dominant and recessive hydroxymethylbilane synthase mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.