Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP815779.RAiBUl2Oi1u4I37JvojK2h1Dab2uTiU1GimHorBC5hWj4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP815779.RAiBUl2Oi1u4I37JvojK2h1Dab2uTiU1GimHorBC5hWj4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP815779.RAiBUl2Oi1u4I37JvojK2h1Dab2uTiU1GimHorBC5hWj4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP815779.RAiBUl2Oi1u4I37JvojK2h1Dab2uTiU1GimHorBC5hWj4130_provenance.
- NP815779.RAiBUl2Oi1u4I37JvojK2h1Dab2uTiU1GimHorBC5hWj4130_assertion description "[Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP815779.RAiBUl2Oi1u4I37JvojK2h1Dab2uTiU1GimHorBC5hWj4130_provenance.
- NP815779.RAiBUl2Oi1u4I37JvojK2h1Dab2uTiU1GimHorBC5hWj4130_assertion evidence source_evidence_literature NP815779.RAiBUl2Oi1u4I37JvojK2h1Dab2uTiU1GimHorBC5hWj4130_provenance.
- NP815779.RAiBUl2Oi1u4I37JvojK2h1Dab2uTiU1GimHorBC5hWj4130_assertion SIO_000772 23623389 NP815779.RAiBUl2Oi1u4I37JvojK2h1Dab2uTiU1GimHorBC5hWj4130_provenance.
- NP815779.RAiBUl2Oi1u4I37JvojK2h1Dab2uTiU1GimHorBC5hWj4130_assertion wasDerivedFrom befree-20140225 NP815779.RAiBUl2Oi1u4I37JvojK2h1Dab2uTiU1GimHorBC5hWj4130_provenance.
- NP815779.RAiBUl2Oi1u4I37JvojK2h1Dab2uTiU1GimHorBC5hWj4130_assertion wasGeneratedBy ECO_0000203 NP815779.RAiBUl2Oi1u4I37JvojK2h1Dab2uTiU1GimHorBC5hWj4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP815779.RAiBUl2Oi1u4I37JvojK2h1Dab2uTiU1GimHorBC5hWj4130_provenance.