Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP383669.RAzovSptZwNXli3N-lty6r4CDB0uweqIf1buXfJprVmvY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP383669.RAzovSptZwNXli3N-lty6r4CDB0uweqIf1buXfJprVmvY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP383669.RAzovSptZwNXli3N-lty6r4CDB0uweqIf1buXfJprVmvY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP383669.RAzovSptZwNXli3N-lty6r4CDB0uweqIf1buXfJprVmvY130_provenance.
- NP383669.RAzovSptZwNXli3N-lty6r4CDB0uweqIf1buXfJprVmvY130_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." NP383669.RAzovSptZwNXli3N-lty6r4CDB0uweqIf1buXfJprVmvY130_provenance.
- NP383669.RAzovSptZwNXli3N-lty6r4CDB0uweqIf1buXfJprVmvY130_assertion evidence source_evidence_literature NP383669.RAzovSptZwNXli3N-lty6r4CDB0uweqIf1buXfJprVmvY130_provenance.
- NP383669.RAzovSptZwNXli3N-lty6r4CDB0uweqIf1buXfJprVmvY130_assertion SIO_000772 7613092 NP383669.RAzovSptZwNXli3N-lty6r4CDB0uweqIf1buXfJprVmvY130_provenance.
- NP383669.RAzovSptZwNXli3N-lty6r4CDB0uweqIf1buXfJprVmvY130_assertion wasDerivedFrom befree-20140225 NP383669.RAzovSptZwNXli3N-lty6r4CDB0uweqIf1buXfJprVmvY130_provenance.
- NP383669.RAzovSptZwNXli3N-lty6r4CDB0uweqIf1buXfJprVmvY130_assertion wasGeneratedBy ECO_0000203 NP383669.RAzovSptZwNXli3N-lty6r4CDB0uweqIf1buXfJprVmvY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP383669.RAzovSptZwNXli3N-lty6r4CDB0uweqIf1buXfJprVmvY130_provenance.