Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1386739.RANtz1F61vNAh6GB79_7y-snH0J7JC2XGyvEJMzniNBmU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1386739.RANtz1F61vNAh6GB79_7y-snH0J7JC2XGyvEJMzniNBmU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1386739.RANtz1F61vNAh6GB79_7y-snH0J7JC2XGyvEJMzniNBmU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1386739.RANtz1F61vNAh6GB79_7y-snH0J7JC2XGyvEJMzniNBmU130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1386739.RANtz1F61vNAh6GB79_7y-snH0J7JC2XGyvEJMzniNBmU130_provenance.