Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_provenance.
- NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_assertion description "[These results establish the essential function of the XPD protein in mammals and in cellular viability and are consistent with the notion that only subtle XPD mutations are found in XP, XP/Cockayne syndrome, and trichothiodystrophy patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_provenance.
- NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_assertion evidence source_evidence_literature NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_provenance.
- NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_assertion SIO_000772 9426063 NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_provenance.
- NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_assertion wasDerivedFrom befree-2016 NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_provenance.
- NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_assertion wasGeneratedBy ECO_0000203 NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_provenance.