Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP319570.RAfshkvoAPuIh4ggxz_nwaKWA2GobTXIvx2EbWIbszd-M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP319570.RAfshkvoAPuIh4ggxz_nwaKWA2GobTXIvx2EbWIbszd-M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP319570.RAfshkvoAPuIh4ggxz_nwaKWA2GobTXIvx2EbWIbszd-M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP319570.RAfshkvoAPuIh4ggxz_nwaKWA2GobTXIvx2EbWIbszd-M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP319570.RAfshkvoAPuIh4ggxz_nwaKWA2GobTXIvx2EbWIbszd-M130_provenance.
- NP319570.RAfshkvoAPuIh4ggxz_nwaKWA2GobTXIvx2EbWIbszd-M130_assertion wasGeneratedBy ECO_0000203 NP319570.RAfshkvoAPuIh4ggxz_nwaKWA2GobTXIvx2EbWIbszd-M130_provenance.
- NP319570.RAfshkvoAPuIh4ggxz_nwaKWA2GobTXIvx2EbWIbszd-M130_assertion wasDerivedFrom befree-20150227 NP319570.RAfshkvoAPuIh4ggxz_nwaKWA2GobTXIvx2EbWIbszd-M130_provenance.
- NP319570.RAfshkvoAPuIh4ggxz_nwaKWA2GobTXIvx2EbWIbszd-M130_assertion SIO_000772 14644728 NP319570.RAfshkvoAPuIh4ggxz_nwaKWA2GobTXIvx2EbWIbszd-M130_provenance.
- NP319570.RAfshkvoAPuIh4ggxz_nwaKWA2GobTXIvx2EbWIbszd-M130_assertion evidence source_evidence_literature NP319570.RAfshkvoAPuIh4ggxz_nwaKWA2GobTXIvx2EbWIbszd-M130_provenance.
- NP319570.RAfshkvoAPuIh4ggxz_nwaKWA2GobTXIvx2EbWIbszd-M130_assertion description "[The absence of systemic features was characteristic of the vitreoretinopathies linked to chromosome 5q13 (Wagner disease and erosive vitreoretinopathy) and mutations in exon 2 of the COL2A1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319570.RAfshkvoAPuIh4ggxz_nwaKWA2GobTXIvx2EbWIbszd-M130_provenance.