Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP568399.RASoRC1IPUpWLhVBK8spRGKkijWGlwFyRtlbVN8363nO8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP568399.RASoRC1IPUpWLhVBK8spRGKkijWGlwFyRtlbVN8363nO8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568399.RASoRC1IPUpWLhVBK8spRGKkijWGlwFyRtlbVN8363nO8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568399.RASoRC1IPUpWLhVBK8spRGKkijWGlwFyRtlbVN8363nO8130_provenance.
- NP568399.RASoRC1IPUpWLhVBK8spRGKkijWGlwFyRtlbVN8363nO8130_assertion description "[Here, we report for the first time that mutations in CABP4 lead to autosomal recessive CSNB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568399.RASoRC1IPUpWLhVBK8spRGKkijWGlwFyRtlbVN8363nO8130_provenance.
- NP568399.RASoRC1IPUpWLhVBK8spRGKkijWGlwFyRtlbVN8363nO8130_assertion evidence source_evidence_literature NP568399.RASoRC1IPUpWLhVBK8spRGKkijWGlwFyRtlbVN8363nO8130_provenance.
- NP568399.RASoRC1IPUpWLhVBK8spRGKkijWGlwFyRtlbVN8363nO8130_assertion SIO_000772 16960802 NP568399.RASoRC1IPUpWLhVBK8spRGKkijWGlwFyRtlbVN8363nO8130_provenance.
- NP568399.RASoRC1IPUpWLhVBK8spRGKkijWGlwFyRtlbVN8363nO8130_assertion wasDerivedFrom befree-2016 NP568399.RASoRC1IPUpWLhVBK8spRGKkijWGlwFyRtlbVN8363nO8130_provenance.
- NP568399.RASoRC1IPUpWLhVBK8spRGKkijWGlwFyRtlbVN8363nO8130_assertion wasGeneratedBy ECO_0000203 NP568399.RASoRC1IPUpWLhVBK8spRGKkijWGlwFyRtlbVN8363nO8130_provenance.
- befree-2016 importedOn "2016-02-19" NP568399.RASoRC1IPUpWLhVBK8spRGKkijWGlwFyRtlbVN8363nO8130_provenance.