Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP921426.RAjCftYow7WSDIAImJXhihQr4AhiKwGlyQLgImRkq-uTw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP921426.RAjCftYow7WSDIAImJXhihQr4AhiKwGlyQLgImRkq-uTw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP921426.RAjCftYow7WSDIAImJXhihQr4AhiKwGlyQLgImRkq-uTw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP921426.RAjCftYow7WSDIAImJXhihQr4AhiKwGlyQLgImRkq-uTw130_provenance.
- NP921426.RAjCftYow7WSDIAImJXhihQr4AhiKwGlyQLgImRkq-uTw130_assertion description "[Hypomorphic mutations in NBN (previously known as NBS1) and MRE11A give rise to the autosomal-recessive diseases Nijmegen breakage syndrome (NBS) and ataxia-telangiectasia-like disorder (ATLD), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921426.RAjCftYow7WSDIAImJXhihQr4AhiKwGlyQLgImRkq-uTw130_provenance.
- NP921426.RAjCftYow7WSDIAImJXhihQr4AhiKwGlyQLgImRkq-uTw130_assertion evidence source_evidence_literature NP921426.RAjCftYow7WSDIAImJXhihQr4AhiKwGlyQLgImRkq-uTw130_provenance.
- NP921426.RAjCftYow7WSDIAImJXhihQr4AhiKwGlyQLgImRkq-uTw130_assertion SIO_000772 19409520 NP921426.RAjCftYow7WSDIAImJXhihQr4AhiKwGlyQLgImRkq-uTw130_provenance.
- NP921426.RAjCftYow7WSDIAImJXhihQr4AhiKwGlyQLgImRkq-uTw130_assertion wasDerivedFrom befree-20140225 NP921426.RAjCftYow7WSDIAImJXhihQr4AhiKwGlyQLgImRkq-uTw130_provenance.
- NP921426.RAjCftYow7WSDIAImJXhihQr4AhiKwGlyQLgImRkq-uTw130_assertion wasGeneratedBy ECO_0000203 NP921426.RAjCftYow7WSDIAImJXhihQr4AhiKwGlyQLgImRkq-uTw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP921426.RAjCftYow7WSDIAImJXhihQr4AhiKwGlyQLgImRkq-uTw130_provenance.