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- source_evidence_literature type ECO_0000212 NP992085.RAeUR4rsiSzGC1JGBbsMo8G_BejJEFsoPZJ3DtaVF8Xsw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP992085.RAeUR4rsiSzGC1JGBbsMo8G_BejJEFsoPZJ3DtaVF8Xsw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP992085.RAeUR4rsiSzGC1JGBbsMo8G_BejJEFsoPZJ3DtaVF8Xsw130_provenance.
- NP992085.RAeUR4rsiSzGC1JGBbsMo8G_BejJEFsoPZJ3DtaVF8Xsw130_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." NP992085.RAeUR4rsiSzGC1JGBbsMo8G_BejJEFsoPZJ3DtaVF8Xsw130_provenance.
- NP992085.RAeUR4rsiSzGC1JGBbsMo8G_BejJEFsoPZJ3DtaVF8Xsw130_assertion evidence source_evidence_literature NP992085.RAeUR4rsiSzGC1JGBbsMo8G_BejJEFsoPZJ3DtaVF8Xsw130_provenance.
- NP992085.RAeUR4rsiSzGC1JGBbsMo8G_BejJEFsoPZJ3DtaVF8Xsw130_assertion SIO_000772 7613092 NP992085.RAeUR4rsiSzGC1JGBbsMo8G_BejJEFsoPZJ3DtaVF8Xsw130_provenance.
- NP992085.RAeUR4rsiSzGC1JGBbsMo8G_BejJEFsoPZJ3DtaVF8Xsw130_assertion wasDerivedFrom befree-20150227 NP992085.RAeUR4rsiSzGC1JGBbsMo8G_BejJEFsoPZJ3DtaVF8Xsw130_provenance.
- NP992085.RAeUR4rsiSzGC1JGBbsMo8G_BejJEFsoPZJ3DtaVF8Xsw130_assertion wasGeneratedBy ECO_0000203 NP992085.RAeUR4rsiSzGC1JGBbsMo8G_BejJEFsoPZJ3DtaVF8Xsw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP992085.RAeUR4rsiSzGC1JGBbsMo8G_BejJEFsoPZJ3DtaVF8Xsw130_provenance.