Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1386739.RANtz1F61vNAh6GB79_7y-snH0J7JC2XGyvEJMzniNBmU130_assertion> ?p ?o ?g. }
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- NP1386739.RANtz1F61vNAh6GB79_7y-snH0J7JC2XGyvEJMzniNBmU130_assertion type Assertion NP1386739.RANtz1F61vNAh6GB79_7y-snH0J7JC2XGyvEJMzniNBmU130_head.
- NP1386739.RANtz1F61vNAh6GB79_7y-snH0J7JC2XGyvEJMzniNBmU130_assertion description "[Point mutations in the XPD gene lead either to the cancer-prone repair syndrome XP, sometimes in combination with a second repair condition; Cockayne syndrome; or the non-cancer-prone brittle-hair disorder trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1386739.RANtz1F61vNAh6GB79_7y-snH0J7JC2XGyvEJMzniNBmU130_provenance.
- NP1386739.RANtz1F61vNAh6GB79_7y-snH0J7JC2XGyvEJMzniNBmU130_assertion evidence source_evidence_literature NP1386739.RANtz1F61vNAh6GB79_7y-snH0J7JC2XGyvEJMzniNBmU130_provenance.
- NP1386739.RANtz1F61vNAh6GB79_7y-snH0J7JC2XGyvEJMzniNBmU130_assertion SIO_000772 9426063 NP1386739.RANtz1F61vNAh6GB79_7y-snH0J7JC2XGyvEJMzniNBmU130_provenance.
- NP1386739.RANtz1F61vNAh6GB79_7y-snH0J7JC2XGyvEJMzniNBmU130_assertion wasDerivedFrom befree-2016 NP1386739.RANtz1F61vNAh6GB79_7y-snH0J7JC2XGyvEJMzniNBmU130_provenance.
- NP1386739.RANtz1F61vNAh6GB79_7y-snH0J7JC2XGyvEJMzniNBmU130_assertion wasGeneratedBy ECO_0000203 NP1386739.RANtz1F61vNAh6GB79_7y-snH0J7JC2XGyvEJMzniNBmU130_provenance.