Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP397833.RA6G3NcedEcRhyrRbLriH4m3RyHv2zXMny2Gz_ei6fVIs130_assertion> ?p ?o ?g. }
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- NP397833.RA6G3NcedEcRhyrRbLriH4m3RyHv2zXMny2Gz_ei6fVIs130_assertion type Assertion NP397833.RA6G3NcedEcRhyrRbLriH4m3RyHv2zXMny2Gz_ei6fVIs130_head.
- NP397833.RA6G3NcedEcRhyrRbLriH4m3RyHv2zXMny2Gz_ei6fVIs130_assertion description "[Our observations suggest that the usual explanation for the association of late-onset EPP with MPD and MDS is acquired somatic mutation of one FECH allele in bone marrow and show for the first time that the consequent overproduction of protoporphyrin may be severe enough to cause acute liver damage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP397833.RA6G3NcedEcRhyrRbLriH4m3RyHv2zXMny2Gz_ei6fVIs130_provenance.
- NP397833.RA6G3NcedEcRhyrRbLriH4m3RyHv2zXMny2Gz_ei6fVIs130_assertion evidence source_evidence_literature NP397833.RA6G3NcedEcRhyrRbLriH4m3RyHv2zXMny2Gz_ei6fVIs130_provenance.
- NP397833.RA6G3NcedEcRhyrRbLriH4m3RyHv2zXMny2Gz_ei6fVIs130_assertion SIO_000772 16150949 NP397833.RA6G3NcedEcRhyrRbLriH4m3RyHv2zXMny2Gz_ei6fVIs130_provenance.
- NP397833.RA6G3NcedEcRhyrRbLriH4m3RyHv2zXMny2Gz_ei6fVIs130_assertion wasDerivedFrom befree-20150227 NP397833.RA6G3NcedEcRhyrRbLriH4m3RyHv2zXMny2Gz_ei6fVIs130_provenance.
- NP397833.RA6G3NcedEcRhyrRbLriH4m3RyHv2zXMny2Gz_ei6fVIs130_assertion wasGeneratedBy ECO_0000203 NP397833.RA6G3NcedEcRhyrRbLriH4m3RyHv2zXMny2Gz_ei6fVIs130_provenance.