Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP971744.RAEdaiYnCoh27X4OVRDtczM0UOVWp6uEmjFAj8PYauc0w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP971744.RAEdaiYnCoh27X4OVRDtczM0UOVWp6uEmjFAj8PYauc0w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP971744.RAEdaiYnCoh27X4OVRDtczM0UOVWp6uEmjFAj8PYauc0w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP971744.RAEdaiYnCoh27X4OVRDtczM0UOVWp6uEmjFAj8PYauc0w130_provenance.
- befree-2016 importedOn "2016-02-19" NP971744.RAEdaiYnCoh27X4OVRDtczM0UOVWp6uEmjFAj8PYauc0w130_provenance.
- NP971744.RAEdaiYnCoh27X4OVRDtczM0UOVWp6uEmjFAj8PYauc0w130_assertion wasGeneratedBy ECO_0000203 NP971744.RAEdaiYnCoh27X4OVRDtczM0UOVWp6uEmjFAj8PYauc0w130_provenance.
- NP971744.RAEdaiYnCoh27X4OVRDtczM0UOVWp6uEmjFAj8PYauc0w130_assertion wasDerivedFrom befree-2016 NP971744.RAEdaiYnCoh27X4OVRDtczM0UOVWp6uEmjFAj8PYauc0w130_provenance.
- NP971744.RAEdaiYnCoh27X4OVRDtczM0UOVWp6uEmjFAj8PYauc0w130_assertion SIO_000772 22466610 NP971744.RAEdaiYnCoh27X4OVRDtczM0UOVWp6uEmjFAj8PYauc0w130_provenance.
- NP971744.RAEdaiYnCoh27X4OVRDtczM0UOVWp6uEmjFAj8PYauc0w130_assertion evidence source_evidence_literature NP971744.RAEdaiYnCoh27X4OVRDtczM0UOVWp6uEmjFAj8PYauc0w130_provenance.
- NP971744.RAEdaiYnCoh27X4OVRDtczM0UOVWp6uEmjFAj8PYauc0w130_assertion description "[Three of the seven known UV(S)S cases carry mutations in the Cockayne syndrome genes ERCC8 or ERCC6 (also known as CSA and CSB, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP971744.RAEdaiYnCoh27X4OVRDtczM0UOVWp6uEmjFAj8PYauc0w130_provenance.