Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP783612.RAhWlM-zOTDO42IXZWFDv3rFP7Gvxq9yMhM5gY8azGQek130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783612.RAhWlM-zOTDO42IXZWFDv3rFP7Gvxq9yMhM5gY8azGQek130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783612.RAhWlM-zOTDO42IXZWFDv3rFP7Gvxq9yMhM5gY8azGQek130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783612.RAhWlM-zOTDO42IXZWFDv3rFP7Gvxq9yMhM5gY8azGQek130_provenance.
- NP783612.RAhWlM-zOTDO42IXZWFDv3rFP7Gvxq9yMhM5gY8azGQek130_assertion description "[This report emphasizes concurrently that ABCC6 may be a relevant candidate gene in some cases of GACI with no mutations in the ENPP1 gene, and that GACI may be an atypical and severe end of the vascular phenotype spectrum of PXE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783612.RAhWlM-zOTDO42IXZWFDv3rFP7Gvxq9yMhM5gY8azGQek130_provenance.
- NP783612.RAhWlM-zOTDO42IXZWFDv3rFP7Gvxq9yMhM5gY8azGQek130_assertion evidence source_evidence_literature NP783612.RAhWlM-zOTDO42IXZWFDv3rFP7Gvxq9yMhM5gY8azGQek130_provenance.
- NP783612.RAhWlM-zOTDO42IXZWFDv3rFP7Gvxq9yMhM5gY8azGQek130_assertion SIO_000772 20034067 NP783612.RAhWlM-zOTDO42IXZWFDv3rFP7Gvxq9yMhM5gY8azGQek130_provenance.
- NP783612.RAhWlM-zOTDO42IXZWFDv3rFP7Gvxq9yMhM5gY8azGQek130_assertion wasDerivedFrom befree-2016 NP783612.RAhWlM-zOTDO42IXZWFDv3rFP7Gvxq9yMhM5gY8azGQek130_provenance.
- NP783612.RAhWlM-zOTDO42IXZWFDv3rFP7Gvxq9yMhM5gY8azGQek130_assertion wasGeneratedBy ECO_0000203 NP783612.RAhWlM-zOTDO42IXZWFDv3rFP7Gvxq9yMhM5gY8azGQek130_provenance.
- befree-2016 importedOn "2016-02-19" NP783612.RAhWlM-zOTDO42IXZWFDv3rFP7Gvxq9yMhM5gY8azGQek130_provenance.