Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP318362.RAG5WxGVi27RM_v08ndBAnz7LcFxuI95dKOC-b4VebsAs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP318362.RAG5WxGVi27RM_v08ndBAnz7LcFxuI95dKOC-b4VebsAs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP318362.RAG5WxGVi27RM_v08ndBAnz7LcFxuI95dKOC-b4VebsAs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP318362.RAG5WxGVi27RM_v08ndBAnz7LcFxuI95dKOC-b4VebsAs130_provenance.
- NP318362.RAG5WxGVi27RM_v08ndBAnz7LcFxuI95dKOC-b4VebsAs130_assertion description "[Functional consequences of progressive cone dystrophy-associated mutations in the human cone photoreceptor cyclic nucleotide-gated channel CNGA3 subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP318362.RAG5WxGVi27RM_v08ndBAnz7LcFxuI95dKOC-b4VebsAs130_provenance.
- NP318362.RAG5WxGVi27RM_v08ndBAnz7LcFxuI95dKOC-b4VebsAs130_assertion evidence source_evidence_literature NP318362.RAG5WxGVi27RM_v08ndBAnz7LcFxuI95dKOC-b4VebsAs130_provenance.
- NP318362.RAG5WxGVi27RM_v08ndBAnz7LcFxuI95dKOC-b4VebsAs130_assertion SIO_000772 15743887 NP318362.RAG5WxGVi27RM_v08ndBAnz7LcFxuI95dKOC-b4VebsAs130_provenance.
- NP318362.RAG5WxGVi27RM_v08ndBAnz7LcFxuI95dKOC-b4VebsAs130_assertion wasDerivedFrom befree-20150227 NP318362.RAG5WxGVi27RM_v08ndBAnz7LcFxuI95dKOC-b4VebsAs130_provenance.
- NP318362.RAG5WxGVi27RM_v08ndBAnz7LcFxuI95dKOC-b4VebsAs130_assertion wasGeneratedBy ECO_0000203 NP318362.RAG5WxGVi27RM_v08ndBAnz7LcFxuI95dKOC-b4VebsAs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP318362.RAG5WxGVi27RM_v08ndBAnz7LcFxuI95dKOC-b4VebsAs130_provenance.