Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1315045.RAAbCyjAfleE3bO8YggA4B-smT8m5DqknNIFQqDzNixoY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1315045.RAAbCyjAfleE3bO8YggA4B-smT8m5DqknNIFQqDzNixoY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1315045.RAAbCyjAfleE3bO8YggA4B-smT8m5DqknNIFQqDzNixoY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1315045.RAAbCyjAfleE3bO8YggA4B-smT8m5DqknNIFQqDzNixoY130_provenance.
- NP1315045.RAAbCyjAfleE3bO8YggA4B-smT8m5DqknNIFQqDzNixoY130_assertion description "[The dysfunction of TFIIH could result in a large panel of genetic disorders, such as xeroderma pigmentosum, Cockayne's syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1315045.RAAbCyjAfleE3bO8YggA4B-smT8m5DqknNIFQqDzNixoY130_provenance.
- NP1315045.RAAbCyjAfleE3bO8YggA4B-smT8m5DqknNIFQqDzNixoY130_assertion evidence source_evidence_literature NP1315045.RAAbCyjAfleE3bO8YggA4B-smT8m5DqknNIFQqDzNixoY130_provenance.
- NP1315045.RAAbCyjAfleE3bO8YggA4B-smT8m5DqknNIFQqDzNixoY130_assertion SIO_000772 7613092 NP1315045.RAAbCyjAfleE3bO8YggA4B-smT8m5DqknNIFQqDzNixoY130_provenance.
- NP1315045.RAAbCyjAfleE3bO8YggA4B-smT8m5DqknNIFQqDzNixoY130_assertion wasDerivedFrom befree-2016 NP1315045.RAAbCyjAfleE3bO8YggA4B-smT8m5DqknNIFQqDzNixoY130_provenance.
- NP1315045.RAAbCyjAfleE3bO8YggA4B-smT8m5DqknNIFQqDzNixoY130_assertion wasGeneratedBy ECO_0000203 NP1315045.RAAbCyjAfleE3bO8YggA4B-smT8m5DqknNIFQqDzNixoY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1315045.RAAbCyjAfleE3bO8YggA4B-smT8m5DqknNIFQqDzNixoY130_provenance.