Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP781285.RAzl4teoQ_uemi9OFh7IgOC9EC3K9R9zkVLpZ0MFwS45g130_assertion> ?p ?o ?g. }
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- NP781285.RAzl4teoQ_uemi9OFh7IgOC9EC3K9R9zkVLpZ0MFwS45g130_assertion type Assertion NP781285.RAzl4teoQ_uemi9OFh7IgOC9EC3K9R9zkVLpZ0MFwS45g130_head.
- NP781285.RAzl4teoQ_uemi9OFh7IgOC9EC3K9R9zkVLpZ0MFwS45g130_assertion description "[Hereditary coproporphyria (HC) is an acute hepatic porphyria with autosomal dominant inheritance caused by a deficient activity of coproporphyrinogen IX oxidase (CPX).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781285.RAzl4teoQ_uemi9OFh7IgOC9EC3K9R9zkVLpZ0MFwS45g130_provenance.
- NP781285.RAzl4teoQ_uemi9OFh7IgOC9EC3K9R9zkVLpZ0MFwS45g130_assertion evidence source_evidence_literature NP781285.RAzl4teoQ_uemi9OFh7IgOC9EC3K9R9zkVLpZ0MFwS45g130_provenance.
- NP781285.RAzl4teoQ_uemi9OFh7IgOC9EC3K9R9zkVLpZ0MFwS45g130_assertion SIO_000772 7757079 NP781285.RAzl4teoQ_uemi9OFh7IgOC9EC3K9R9zkVLpZ0MFwS45g130_provenance.
- NP781285.RAzl4teoQ_uemi9OFh7IgOC9EC3K9R9zkVLpZ0MFwS45g130_assertion wasDerivedFrom befree-20140225 NP781285.RAzl4teoQ_uemi9OFh7IgOC9EC3K9R9zkVLpZ0MFwS45g130_provenance.
- NP781285.RAzl4teoQ_uemi9OFh7IgOC9EC3K9R9zkVLpZ0MFwS45g130_assertion wasGeneratedBy ECO_0000203 NP781285.RAzl4teoQ_uemi9OFh7IgOC9EC3K9R9zkVLpZ0MFwS45g130_provenance.