Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP990285.RAeKOLFYgUIXmXkOc2TeBLiKh8g7BVMqtlbINq0Agu1_g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP990285.RAeKOLFYgUIXmXkOc2TeBLiKh8g7BVMqtlbINq0Agu1_g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP990285.RAeKOLFYgUIXmXkOc2TeBLiKh8g7BVMqtlbINq0Agu1_g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP990285.RAeKOLFYgUIXmXkOc2TeBLiKh8g7BVMqtlbINq0Agu1_g130_provenance.
- NP990285.RAeKOLFYgUIXmXkOc2TeBLiKh8g7BVMqtlbINq0Agu1_g130_assertion description "[Novel mutations and electrophysiologic findings in RGS9- and R9AP-associated retinal dysfunction (Bradyopsia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990285.RAeKOLFYgUIXmXkOc2TeBLiKh8g7BVMqtlbINq0Agu1_g130_provenance.
- NP990285.RAeKOLFYgUIXmXkOc2TeBLiKh8g7BVMqtlbINq0Agu1_g130_assertion evidence source_evidence_literature NP990285.RAeKOLFYgUIXmXkOc2TeBLiKh8g7BVMqtlbINq0Agu1_g130_provenance.
- NP990285.RAeKOLFYgUIXmXkOc2TeBLiKh8g7BVMqtlbINq0Agu1_g130_assertion SIO_000772 19818506 NP990285.RAeKOLFYgUIXmXkOc2TeBLiKh8g7BVMqtlbINq0Agu1_g130_provenance.
- NP990285.RAeKOLFYgUIXmXkOc2TeBLiKh8g7BVMqtlbINq0Agu1_g130_assertion wasDerivedFrom befree-20150227 NP990285.RAeKOLFYgUIXmXkOc2TeBLiKh8g7BVMqtlbINq0Agu1_g130_provenance.
- NP990285.RAeKOLFYgUIXmXkOc2TeBLiKh8g7BVMqtlbINq0Agu1_g130_assertion wasGeneratedBy ECO_0000203 NP990285.RAeKOLFYgUIXmXkOc2TeBLiKh8g7BVMqtlbINq0Agu1_g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP990285.RAeKOLFYgUIXmXkOc2TeBLiKh8g7BVMqtlbINq0Agu1_g130_provenance.