Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP462747.RA2xMsWvjVBcTpL9KgO3SGbu2bm-MCAITYNfWKvUCn58o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP462747.RA2xMsWvjVBcTpL9KgO3SGbu2bm-MCAITYNfWKvUCn58o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP462747.RA2xMsWvjVBcTpL9KgO3SGbu2bm-MCAITYNfWKvUCn58o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP462747.RA2xMsWvjVBcTpL9KgO3SGbu2bm-MCAITYNfWKvUCn58o130_provenance.
- befree-2016 importedOn "2016-02-19" NP462747.RA2xMsWvjVBcTpL9KgO3SGbu2bm-MCAITYNfWKvUCn58o130_provenance.
- NP462747.RA2xMsWvjVBcTpL9KgO3SGbu2bm-MCAITYNfWKvUCn58o130_assertion wasGeneratedBy ECO_0000203 NP462747.RA2xMsWvjVBcTpL9KgO3SGbu2bm-MCAITYNfWKvUCn58o130_provenance.
- NP462747.RA2xMsWvjVBcTpL9KgO3SGbu2bm-MCAITYNfWKvUCn58o130_assertion wasDerivedFrom befree-2016 NP462747.RA2xMsWvjVBcTpL9KgO3SGbu2bm-MCAITYNfWKvUCn58o130_provenance.
- NP462747.RA2xMsWvjVBcTpL9KgO3SGbu2bm-MCAITYNfWKvUCn58o130_assertion SIO_000772 15459175 NP462747.RA2xMsWvjVBcTpL9KgO3SGbu2bm-MCAITYNfWKvUCn58o130_provenance.
- NP462747.RA2xMsWvjVBcTpL9KgO3SGbu2bm-MCAITYNfWKvUCn58o130_assertion evidence source_evidence_literature NP462747.RA2xMsWvjVBcTpL9KgO3SGbu2bm-MCAITYNfWKvUCn58o130_provenance.
- NP462747.RA2xMsWvjVBcTpL9KgO3SGbu2bm-MCAITYNfWKvUCn58o130_assertion description "[RAI1 has been recently suggested as a major gene for majority of the SMS phenotypes, but its role in the full spectrum of the phenotype remains unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP462747.RA2xMsWvjVBcTpL9KgO3SGbu2bm-MCAITYNfWKvUCn58o130_provenance.