Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP362492.RA7iyFFiey0IpChNZDgw2sqwlO9NxglrKPiqF-XtEgKug130_assertion> ?p ?o ?g. }
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- NP362492.RA7iyFFiey0IpChNZDgw2sqwlO9NxglrKPiqF-XtEgKug130_assertion type Assertion NP362492.RA7iyFFiey0IpChNZDgw2sqwlO9NxglrKPiqF-XtEgKug130_head.
- NP362492.RA7iyFFiey0IpChNZDgw2sqwlO9NxglrKPiqF-XtEgKug130_assertion wasGeneratedBy ECO_0000203 NP362492.RA7iyFFiey0IpChNZDgw2sqwlO9NxglrKPiqF-XtEgKug130_provenance.
- NP362492.RA7iyFFiey0IpChNZDgw2sqwlO9NxglrKPiqF-XtEgKug130_assertion wasDerivedFrom befree-20140225 NP362492.RA7iyFFiey0IpChNZDgw2sqwlO9NxglrKPiqF-XtEgKug130_provenance.
- NP362492.RA7iyFFiey0IpChNZDgw2sqwlO9NxglrKPiqF-XtEgKug130_assertion SIO_000772 20687508 NP362492.RA7iyFFiey0IpChNZDgw2sqwlO9NxglrKPiqF-XtEgKug130_provenance.
- NP362492.RA7iyFFiey0IpChNZDgw2sqwlO9NxglrKPiqF-XtEgKug130_assertion evidence source_evidence_literature NP362492.RA7iyFFiey0IpChNZDgw2sqwlO9NxglrKPiqF-XtEgKug130_provenance.
- NP362492.RA7iyFFiey0IpChNZDgw2sqwlO9NxglrKPiqF-XtEgKug130_assertion description "[This syndrome is now recognized as a disorder belonging to the spectrum of inherited defects in Nucleotide Excision Repair (NER) resulting in profound photosensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362492.RA7iyFFiey0IpChNZDgw2sqwlO9NxglrKPiqF-XtEgKug130_provenance.