Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1011276.RAcCkRRcoCMiliH-I4JX_uVML76bxIZkZQxcbxgq_zFhA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1011276.RAcCkRRcoCMiliH-I4JX_uVML76bxIZkZQxcbxgq_zFhA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1011276.RAcCkRRcoCMiliH-I4JX_uVML76bxIZkZQxcbxgq_zFhA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1011276.RAcCkRRcoCMiliH-I4JX_uVML76bxIZkZQxcbxgq_zFhA130_provenance.
- NP1011276.RAcCkRRcoCMiliH-I4JX_uVML76bxIZkZQxcbxgq_zFhA130_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." NP1011276.RAcCkRRcoCMiliH-I4JX_uVML76bxIZkZQxcbxgq_zFhA130_provenance.
- NP1011276.RAcCkRRcoCMiliH-I4JX_uVML76bxIZkZQxcbxgq_zFhA130_assertion evidence source_evidence_literature NP1011276.RAcCkRRcoCMiliH-I4JX_uVML76bxIZkZQxcbxgq_zFhA130_provenance.
- NP1011276.RAcCkRRcoCMiliH-I4JX_uVML76bxIZkZQxcbxgq_zFhA130_assertion SIO_000772 16947863 NP1011276.RAcCkRRcoCMiliH-I4JX_uVML76bxIZkZQxcbxgq_zFhA130_provenance.
- NP1011276.RAcCkRRcoCMiliH-I4JX_uVML76bxIZkZQxcbxgq_zFhA130_assertion wasDerivedFrom befree-20150227 NP1011276.RAcCkRRcoCMiliH-I4JX_uVML76bxIZkZQxcbxgq_zFhA130_provenance.
- NP1011276.RAcCkRRcoCMiliH-I4JX_uVML76bxIZkZQxcbxgq_zFhA130_assertion wasGeneratedBy ECO_0000203 NP1011276.RAcCkRRcoCMiliH-I4JX_uVML76bxIZkZQxcbxgq_zFhA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1011276.RAcCkRRcoCMiliH-I4JX_uVML76bxIZkZQxcbxgq_zFhA130_provenance.