Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP263015.RABQXsoL38NTn31nngCG8mL5PVrdOcPQsp7sFMJLTIbFo130_assertion> ?p ?o ?g. }
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- NP263015.RABQXsoL38NTn31nngCG8mL5PVrdOcPQsp7sFMJLTIbFo130_assertion type Assertion NP263015.RABQXsoL38NTn31nngCG8mL5PVrdOcPQsp7sFMJLTIbFo130_head.
- NP263015.RABQXsoL38NTn31nngCG8mL5PVrdOcPQsp7sFMJLTIbFo130_assertion description "[Variegate porphyria (VP) is a low-penetrance, autosomal dominant disorder characterized clinically by skin lesions and acute neurovisceral attacks that occur separately or together.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263015.RABQXsoL38NTn31nngCG8mL5PVrdOcPQsp7sFMJLTIbFo130_provenance.
- NP263015.RABQXsoL38NTn31nngCG8mL5PVrdOcPQsp7sFMJLTIbFo130_assertion evidence source_evidence_literature NP263015.RABQXsoL38NTn31nngCG8mL5PVrdOcPQsp7sFMJLTIbFo130_provenance.
- NP263015.RABQXsoL38NTn31nngCG8mL5PVrdOcPQsp7sFMJLTIbFo130_assertion SIO_000772 10486317 NP263015.RABQXsoL38NTn31nngCG8mL5PVrdOcPQsp7sFMJLTIbFo130_provenance.
- NP263015.RABQXsoL38NTn31nngCG8mL5PVrdOcPQsp7sFMJLTIbFo130_assertion wasDerivedFrom befree-2016 NP263015.RABQXsoL38NTn31nngCG8mL5PVrdOcPQsp7sFMJLTIbFo130_provenance.
- NP263015.RABQXsoL38NTn31nngCG8mL5PVrdOcPQsp7sFMJLTIbFo130_assertion wasGeneratedBy ECO_0000203 NP263015.RABQXsoL38NTn31nngCG8mL5PVrdOcPQsp7sFMJLTIbFo130_provenance.