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- NP1293702.RADOfHE6abUYtBlKI3SpudwiAuJmHzGWB3aQykIFzYUQ4130_assertion type Assertion NP1293702.RADOfHE6abUYtBlKI3SpudwiAuJmHzGWB3aQykIFzYUQ4130_head.
- NP1293702.RADOfHE6abUYtBlKI3SpudwiAuJmHzGWB3aQykIFzYUQ4130_assertion description "[We also reveal the structural basis for defects in patients with xeroderma pigmentosum and trichothiodystrophy, with mutations found at the interface between the p62 Anchor region and the XPD subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293702.RADOfHE6abUYtBlKI3SpudwiAuJmHzGWB3aQykIFzYUQ4130_provenance.
- NP1293702.RADOfHE6abUYtBlKI3SpudwiAuJmHzGWB3aQykIFzYUQ4130_assertion evidence source_evidence_literature NP1293702.RADOfHE6abUYtBlKI3SpudwiAuJmHzGWB3aQykIFzYUQ4130_provenance.
- NP1293702.RADOfHE6abUYtBlKI3SpudwiAuJmHzGWB3aQykIFzYUQ4130_assertion SIO_000772 26340423 NP1293702.RADOfHE6abUYtBlKI3SpudwiAuJmHzGWB3aQykIFzYUQ4130_provenance.
- NP1293702.RADOfHE6abUYtBlKI3SpudwiAuJmHzGWB3aQykIFzYUQ4130_assertion wasDerivedFrom befree-2016 NP1293702.RADOfHE6abUYtBlKI3SpudwiAuJmHzGWB3aQykIFzYUQ4130_provenance.
- NP1293702.RADOfHE6abUYtBlKI3SpudwiAuJmHzGWB3aQykIFzYUQ4130_assertion wasGeneratedBy ECO_0000203 NP1293702.RADOfHE6abUYtBlKI3SpudwiAuJmHzGWB3aQykIFzYUQ4130_provenance.