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- NP1376243.RAcejTSp0hcgic9LSa550aLcS0CHXPSzVO07SOYwfNNXU130_assertion type Assertion NP1376243.RAcejTSp0hcgic9LSa550aLcS0CHXPSzVO07SOYwfNNXU130_head.
- NP1376243.RAcejTSp0hcgic9LSa550aLcS0CHXPSzVO07SOYwfNNXU130_assertion wasGeneratedBy ECO_0000203 NP1376243.RAcejTSp0hcgic9LSa550aLcS0CHXPSzVO07SOYwfNNXU130_provenance.
- NP1376243.RAcejTSp0hcgic9LSa550aLcS0CHXPSzVO07SOYwfNNXU130_assertion wasDerivedFrom befree-2016 NP1376243.RAcejTSp0hcgic9LSa550aLcS0CHXPSzVO07SOYwfNNXU130_provenance.
- NP1376243.RAcejTSp0hcgic9LSa550aLcS0CHXPSzVO07SOYwfNNXU130_assertion SIO_000772 9211196 NP1376243.RAcejTSp0hcgic9LSa550aLcS0CHXPSzVO07SOYwfNNXU130_provenance.
- NP1376243.RAcejTSp0hcgic9LSa550aLcS0CHXPSzVO07SOYwfNNXU130_assertion evidence source_evidence_literature NP1376243.RAcejTSp0hcgic9LSa550aLcS0CHXPSzVO07SOYwfNNXU130_provenance.
- NP1376243.RAcejTSp0hcgic9LSa550aLcS0CHXPSzVO07SOYwfNNXU130_assertion description "[Hepatoerythropoietic porphyria usually develops before the age of 2 years; patients are homo- or heteroallelic for uroporphyrinogen decarboxylase mutations, at least one of which is known to cause type II PCT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1376243.RAcejTSp0hcgic9LSa550aLcS0CHXPSzVO07SOYwfNNXU130_provenance.