Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP638799.RACtLWl_3NAqiOQGO_P-RuU5WMzjwWzURFR3ah4j_2lJo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP638799.RACtLWl_3NAqiOQGO_P-RuU5WMzjwWzURFR3ah4j_2lJo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP638799.RACtLWl_3NAqiOQGO_P-RuU5WMzjwWzURFR3ah4j_2lJo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP638799.RACtLWl_3NAqiOQGO_P-RuU5WMzjwWzURFR3ah4j_2lJo130_provenance.
- NP638799.RACtLWl_3NAqiOQGO_P-RuU5WMzjwWzURFR3ah4j_2lJo130_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." NP638799.RACtLWl_3NAqiOQGO_P-RuU5WMzjwWzURFR3ah4j_2lJo130_provenance.
- NP638799.RACtLWl_3NAqiOQGO_P-RuU5WMzjwWzURFR3ah4j_2lJo130_assertion evidence source_evidence_literature NP638799.RACtLWl_3NAqiOQGO_P-RuU5WMzjwWzURFR3ah4j_2lJo130_provenance.
- NP638799.RACtLWl_3NAqiOQGO_P-RuU5WMzjwWzURFR3ah4j_2lJo130_assertion SIO_000772 7613092 NP638799.RACtLWl_3NAqiOQGO_P-RuU5WMzjwWzURFR3ah4j_2lJo130_provenance.
- NP638799.RACtLWl_3NAqiOQGO_P-RuU5WMzjwWzURFR3ah4j_2lJo130_assertion wasDerivedFrom befree-20140225 NP638799.RACtLWl_3NAqiOQGO_P-RuU5WMzjwWzURFR3ah4j_2lJo130_provenance.
- NP638799.RACtLWl_3NAqiOQGO_P-RuU5WMzjwWzURFR3ah4j_2lJo130_assertion wasGeneratedBy ECO_0000203 NP638799.RACtLWl_3NAqiOQGO_P-RuU5WMzjwWzURFR3ah4j_2lJo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP638799.RACtLWl_3NAqiOQGO_P-RuU5WMzjwWzURFR3ah4j_2lJo130_provenance.