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- source_evidence_literature type ECO_0000212 NP992102.RAEWTKN4A4ewdgAO-k1rAsyYU2i6zrSbIChG_J0DjSnRs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP992102.RAEWTKN4A4ewdgAO-k1rAsyYU2i6zrSbIChG_J0DjSnRs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP992102.RAEWTKN4A4ewdgAO-k1rAsyYU2i6zrSbIChG_J0DjSnRs130_provenance.
- NP992102.RAEWTKN4A4ewdgAO-k1rAsyYU2i6zrSbIChG_J0DjSnRs130_assertion description "[Defects in the xeroderma pigmentosum type B (XPB) gene (ERCC3), a DNA helicase involved in nucleotide excision repair (NER) and an essential subunit of the basal transcription factor, TFIIH, have been described in only three families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP992102.RAEWTKN4A4ewdgAO-k1rAsyYU2i6zrSbIChG_J0DjSnRs130_provenance.
- NP992102.RAEWTKN4A4ewdgAO-k1rAsyYU2i6zrSbIChG_J0DjSnRs130_assertion evidence source_evidence_literature NP992102.RAEWTKN4A4ewdgAO-k1rAsyYU2i6zrSbIChG_J0DjSnRs130_provenance.
- NP992102.RAEWTKN4A4ewdgAO-k1rAsyYU2i6zrSbIChG_J0DjSnRs130_assertion SIO_000772 16947863 NP992102.RAEWTKN4A4ewdgAO-k1rAsyYU2i6zrSbIChG_J0DjSnRs130_provenance.
- NP992102.RAEWTKN4A4ewdgAO-k1rAsyYU2i6zrSbIChG_J0DjSnRs130_assertion wasDerivedFrom befree-20150227 NP992102.RAEWTKN4A4ewdgAO-k1rAsyYU2i6zrSbIChG_J0DjSnRs130_provenance.
- NP992102.RAEWTKN4A4ewdgAO-k1rAsyYU2i6zrSbIChG_J0DjSnRs130_assertion wasGeneratedBy ECO_0000203 NP992102.RAEWTKN4A4ewdgAO-k1rAsyYU2i6zrSbIChG_J0DjSnRs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP992102.RAEWTKN4A4ewdgAO-k1rAsyYU2i6zrSbIChG_J0DjSnRs130_provenance.