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- source_evidence_literature type ECO_0000212 NP246910.RAtq35lUlnjHfzTBTp_BuL-STZO3HMABzV1tGb7n4sqnU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP246910.RAtq35lUlnjHfzTBTp_BuL-STZO3HMABzV1tGb7n4sqnU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP246910.RAtq35lUlnjHfzTBTp_BuL-STZO3HMABzV1tGb7n4sqnU130_provenance.
- NP246910.RAtq35lUlnjHfzTBTp_BuL-STZO3HMABzV1tGb7n4sqnU130_assertion description "[This work, in addition to clarifying the role of the various TFIIH subunits, supports the current hypothesis that XP-B/D patients are more likely to suffer from transcription repair syndromes rather than DNA repair disorders alone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP246910.RAtq35lUlnjHfzTBTp_BuL-STZO3HMABzV1tGb7n4sqnU130_provenance.
- NP246910.RAtq35lUlnjHfzTBTp_BuL-STZO3HMABzV1tGb7n4sqnU130_assertion evidence source_evidence_literature NP246910.RAtq35lUlnjHfzTBTp_BuL-STZO3HMABzV1tGb7n4sqnU130_provenance.
- NP246910.RAtq35lUlnjHfzTBTp_BuL-STZO3HMABzV1tGb7n4sqnU130_assertion SIO_000772 10064601 NP246910.RAtq35lUlnjHfzTBTp_BuL-STZO3HMABzV1tGb7n4sqnU130_provenance.
- NP246910.RAtq35lUlnjHfzTBTp_BuL-STZO3HMABzV1tGb7n4sqnU130_assertion wasDerivedFrom befree-2016 NP246910.RAtq35lUlnjHfzTBTp_BuL-STZO3HMABzV1tGb7n4sqnU130_provenance.
- NP246910.RAtq35lUlnjHfzTBTp_BuL-STZO3HMABzV1tGb7n4sqnU130_assertion wasGeneratedBy ECO_0000203 NP246910.RAtq35lUlnjHfzTBTp_BuL-STZO3HMABzV1tGb7n4sqnU130_provenance.
- befree-2016 importedOn "2016-02-19" NP246910.RAtq35lUlnjHfzTBTp_BuL-STZO3HMABzV1tGb7n4sqnU130_provenance.