Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP749169.RAFo1HFLbmN3DvMQT-zvp-jQR2rpxOODfG7LlgLHYDBUE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP749169.RAFo1HFLbmN3DvMQT-zvp-jQR2rpxOODfG7LlgLHYDBUE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP749169.RAFo1HFLbmN3DvMQT-zvp-jQR2rpxOODfG7LlgLHYDBUE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP749169.RAFo1HFLbmN3DvMQT-zvp-jQR2rpxOODfG7LlgLHYDBUE130_provenance.
- NP749169.RAFo1HFLbmN3DvMQT-zvp-jQR2rpxOODfG7LlgLHYDBUE130_assertion description "[High recurrence of the R1006C NOTCH3 mutation in central Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749169.RAFo1HFLbmN3DvMQT-zvp-jQR2rpxOODfG7LlgLHYDBUE130_provenance.
- NP749169.RAFo1HFLbmN3DvMQT-zvp-jQR2rpxOODfG7LlgLHYDBUE130_assertion evidence source_evidence_literature NP749169.RAFo1HFLbmN3DvMQT-zvp-jQR2rpxOODfG7LlgLHYDBUE130_provenance.
- NP749169.RAFo1HFLbmN3DvMQT-zvp-jQR2rpxOODfG7LlgLHYDBUE130_assertion SIO_000772 19576955 NP749169.RAFo1HFLbmN3DvMQT-zvp-jQR2rpxOODfG7LlgLHYDBUE130_provenance.
- NP749169.RAFo1HFLbmN3DvMQT-zvp-jQR2rpxOODfG7LlgLHYDBUE130_assertion wasDerivedFrom befree-2016 NP749169.RAFo1HFLbmN3DvMQT-zvp-jQR2rpxOODfG7LlgLHYDBUE130_provenance.
- NP749169.RAFo1HFLbmN3DvMQT-zvp-jQR2rpxOODfG7LlgLHYDBUE130_assertion wasGeneratedBy ECO_0000203 NP749169.RAFo1HFLbmN3DvMQT-zvp-jQR2rpxOODfG7LlgLHYDBUE130_provenance.
- befree-2016 importedOn "2016-02-19" NP749169.RAFo1HFLbmN3DvMQT-zvp-jQR2rpxOODfG7LlgLHYDBUE130_provenance.