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- source_evidence_literature type ECO_0000212 NP1386738.RAa67w0EH31ooUpfItyDj8Dsl_Mg5xM6yRdB0QdXAc0LY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1386738.RAa67w0EH31ooUpfItyDj8Dsl_Mg5xM6yRdB0QdXAc0LY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1386738.RAa67w0EH31ooUpfItyDj8Dsl_Mg5xM6yRdB0QdXAc0LY130_provenance.
- NP1386738.RAa67w0EH31ooUpfItyDj8Dsl_Mg5xM6yRdB0QdXAc0LY130_assertion description "[These results establish the essential function of the XPD protein in mammals and in cellular viability and are consistent with the notion that only subtle XPD mutations are found in XP, XP/Cockayne syndrome, and trichothiodystrophy patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1386738.RAa67w0EH31ooUpfItyDj8Dsl_Mg5xM6yRdB0QdXAc0LY130_provenance.
- NP1386738.RAa67w0EH31ooUpfItyDj8Dsl_Mg5xM6yRdB0QdXAc0LY130_assertion evidence source_evidence_literature NP1386738.RAa67w0EH31ooUpfItyDj8Dsl_Mg5xM6yRdB0QdXAc0LY130_provenance.
- NP1386738.RAa67w0EH31ooUpfItyDj8Dsl_Mg5xM6yRdB0QdXAc0LY130_assertion SIO_000772 9426063 NP1386738.RAa67w0EH31ooUpfItyDj8Dsl_Mg5xM6yRdB0QdXAc0LY130_provenance.
- NP1386738.RAa67w0EH31ooUpfItyDj8Dsl_Mg5xM6yRdB0QdXAc0LY130_assertion wasDerivedFrom befree-2016 NP1386738.RAa67w0EH31ooUpfItyDj8Dsl_Mg5xM6yRdB0QdXAc0LY130_provenance.
- NP1386738.RAa67w0EH31ooUpfItyDj8Dsl_Mg5xM6yRdB0QdXAc0LY130_assertion wasGeneratedBy ECO_0000203 NP1386738.RAa67w0EH31ooUpfItyDj8Dsl_Mg5xM6yRdB0QdXAc0LY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1386738.RAa67w0EH31ooUpfItyDj8Dsl_Mg5xM6yRdB0QdXAc0LY130_provenance.