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<http://rdf.disgenet.org/resource/nanopub/NP908344.RA-p-0k1E2F34CCNepdOR_QcfGE15Dwq_EMes0yvee3Nc> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.nanopub.org/nschema#Nanopublication> <http://rdf.disgenet.org/resource/nanopub/NP908344.RA-p-0k1E2F34CCNepdOR_QcfGE15Dwq_EMes0yvee3Nc130_head> .
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<http://identifiers.org/ncbigene/51750> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C16612> <http://rdf.disgenet.org/resource/nanopub/NP908344.RA-p-0k1E2F34CCNepdOR_QcfGE15Dwq_EMes0yvee3Nc130_assertion> .
<http://linkedlifedata.com/resource/umls/id/C0043346> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C7057> <http://rdf.disgenet.org/resource/nanopub/NP908344.RA-p-0k1E2F34CCNepdOR_QcfGE15Dwq_EMes0yvee3Nc130_assertion> .
<http://rdf.disgenet.org/resource/gda/DGN26c1c09b9d5e4bad87d1594459c4c8e4> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/ncbigene/51750> <http://rdf.disgenet.org/resource/nanopub/NP908344.RA-p-0k1E2F34CCNepdOR_QcfGE15Dwq_EMes0yvee3Nc130_assertion> .
<http://rdf.disgenet.org/resource/gda/DGN26c1c09b9d5e4bad87d1594459c4c8e4> <http://semanticscience.org/resource/SIO_000628> <http://linkedlifedata.com/resource/umls/id/C0043346> <http://rdf.disgenet.org/resource/nanopub/NP908344.RA-p-0k1E2F34CCNepdOR_QcfGE15Dwq_EMes0yvee3Nc130_assertion> .
<http://rdf.disgenet.org/resource/gda/DGN26c1c09b9d5e4bad87d1594459c4c8e4> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_001121> <http://rdf.disgenet.org/resource/nanopub/NP908344.RA-p-0k1E2F34CCNepdOR_QcfGE15Dwq_EMes0yvee3Nc130_assertion> .
<http://rdf.disgenet.org/resource/nanopub/NP908344.RA-p-0k1E2F34CCNepdOR_QcfGE15Dwq_EMes0yvee3Nc130_assertion> <http://purl.org/dc/terms/description> "[FANCJ belongs to a conserved iron-sulfur (Fe S) cluster family of helicases important for genomic stability including XPD (nucleotide excision repair), DDX11 (sister chromatid cohesion), and RTEL (telomere metabolism), genetically linked to xeroderma pigmentosum/Cockayne syndrome, Warsaw breakage syndrome, and dyskeratosis congenita, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en <http://rdf.disgenet.org/resource/nanopub/NP908344.RA-p-0k1E2F34CCNepdOR_QcfGE15Dwq_EMes0yvee3Nc130_provenance> .
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<http://rdf.disgenet.org/v3.0.0/void/befree-20150227> <http://purl.org/pav/importedOn> "2015-02-27"^^<http://www.w3.org/2001/XMLSchema#date> <http://rdf.disgenet.org/resource/nanopub/NP908344.RA-p-0k1E2F34CCNepdOR_QcfGE15Dwq_EMes0yvee3Nc130_provenance> .
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<http://rdf.disgenet.org/v3.0.0/void/source_evidence_literature> <http://www.w3.org/2000/01/rdf-schema#comment> "Gene-disease associations inferred from text-mining the literature."@en <http://rdf.disgenet.org/resource/nanopub/NP908344.RA-p-0k1E2F34CCNepdOR_QcfGE15Dwq_EMes0yvee3Nc130_provenance> .
<http://rdf.disgenet.org/v3.0.0/void/source_evidence_literature> <http://www.w3.org/2000/01/rdf-schema#label> "DisGeNET evidence - LITERATURE"@en <http://rdf.disgenet.org/resource/nanopub/NP908344.RA-p-0k1E2F34CCNepdOR_QcfGE15Dwq_EMes0yvee3Nc130_provenance> .
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