Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP222069.RAEa_os57e65YIgFY7nSkWMyoxCu8k4tCCv2N02-tOCiA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP222069.RAEa_os57e65YIgFY7nSkWMyoxCu8k4tCCv2N02-tOCiA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP222069.RAEa_os57e65YIgFY7nSkWMyoxCu8k4tCCv2N02-tOCiA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP222069.RAEa_os57e65YIgFY7nSkWMyoxCu8k4tCCv2N02-tOCiA130_provenance.
- NP222069.RAEa_os57e65YIgFY7nSkWMyoxCu8k4tCCv2N02-tOCiA130_assertion description "[An inherited, late-onset form of kidney failure is caused by point mutations in the alpha-actinin-4 actin-binding domain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222069.RAEa_os57e65YIgFY7nSkWMyoxCu8k4tCCv2N02-tOCiA130_provenance.
- NP222069.RAEa_os57e65YIgFY7nSkWMyoxCu8k4tCCv2N02-tOCiA130_assertion evidence source_evidence_literature NP222069.RAEa_os57e65YIgFY7nSkWMyoxCu8k4tCCv2N02-tOCiA130_provenance.
- NP222069.RAEa_os57e65YIgFY7nSkWMyoxCu8k4tCCv2N02-tOCiA130_assertion SIO_000772 17901210 NP222069.RAEa_os57e65YIgFY7nSkWMyoxCu8k4tCCv2N02-tOCiA130_provenance.
- NP222069.RAEa_os57e65YIgFY7nSkWMyoxCu8k4tCCv2N02-tOCiA130_assertion wasDerivedFrom befree-20150227 NP222069.RAEa_os57e65YIgFY7nSkWMyoxCu8k4tCCv2N02-tOCiA130_provenance.
- NP222069.RAEa_os57e65YIgFY7nSkWMyoxCu8k4tCCv2N02-tOCiA130_assertion wasGeneratedBy ECO_0000203 NP222069.RAEa_os57e65YIgFY7nSkWMyoxCu8k4tCCv2N02-tOCiA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP222069.RAEa_os57e65YIgFY7nSkWMyoxCu8k4tCCv2N02-tOCiA130_provenance.