Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1011257.RAiN7dJ-JXlOTQ27da0Hohxzht17-kwWW6rnrF7JktoCU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1011257.RAiN7dJ-JXlOTQ27da0Hohxzht17-kwWW6rnrF7JktoCU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1011257.RAiN7dJ-JXlOTQ27da0Hohxzht17-kwWW6rnrF7JktoCU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1011257.RAiN7dJ-JXlOTQ27da0Hohxzht17-kwWW6rnrF7JktoCU130_provenance.
- NP1011257.RAiN7dJ-JXlOTQ27da0Hohxzht17-kwWW6rnrF7JktoCU130_assertion description "[In contrast, mutations in two members of the TFIIH complex, the XPB and XPD genes are generally very severe with both skin and CNS disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011257.RAiN7dJ-JXlOTQ27da0Hohxzht17-kwWW6rnrF7JktoCU130_provenance.
- NP1011257.RAiN7dJ-JXlOTQ27da0Hohxzht17-kwWW6rnrF7JktoCU130_assertion evidence source_evidence_literature NP1011257.RAiN7dJ-JXlOTQ27da0Hohxzht17-kwWW6rnrF7JktoCU130_provenance.
- NP1011257.RAiN7dJ-JXlOTQ27da0Hohxzht17-kwWW6rnrF7JktoCU130_assertion SIO_000772 10699759 NP1011257.RAiN7dJ-JXlOTQ27da0Hohxzht17-kwWW6rnrF7JktoCU130_provenance.
- NP1011257.RAiN7dJ-JXlOTQ27da0Hohxzht17-kwWW6rnrF7JktoCU130_assertion wasDerivedFrom befree-20150227 NP1011257.RAiN7dJ-JXlOTQ27da0Hohxzht17-kwWW6rnrF7JktoCU130_provenance.
- NP1011257.RAiN7dJ-JXlOTQ27da0Hohxzht17-kwWW6rnrF7JktoCU130_assertion wasGeneratedBy ECO_0000203 NP1011257.RAiN7dJ-JXlOTQ27da0Hohxzht17-kwWW6rnrF7JktoCU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1011257.RAiN7dJ-JXlOTQ27da0Hohxzht17-kwWW6rnrF7JktoCU130_provenance.