Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP430145.RAIxq5WfdIUkCF8VF_sd8BS2BbgkmTaZAfCYB8sLr5k_4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP430145.RAIxq5WfdIUkCF8VF_sd8BS2BbgkmTaZAfCYB8sLr5k_4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP430145.RAIxq5WfdIUkCF8VF_sd8BS2BbgkmTaZAfCYB8sLr5k_4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP430145.RAIxq5WfdIUkCF8VF_sd8BS2BbgkmTaZAfCYB8sLr5k_4130_provenance.
- NP430145.RAIxq5WfdIUkCF8VF_sd8BS2BbgkmTaZAfCYB8sLr5k_4130_assertion description "[The results indicate that GNB3 and GNGT2 are unlikely sites of mutations responsible for inherited retinal degenerations that predominantly effect cone-mediated function (cone and cone-rod dystrophies) or have a predilection for disease in the macula (macular dystrophies).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430145.RAIxq5WfdIUkCF8VF_sd8BS2BbgkmTaZAfCYB8sLr5k_4130_provenance.
- NP430145.RAIxq5WfdIUkCF8VF_sd8BS2BbgkmTaZAfCYB8sLr5k_4130_assertion evidence source_evidence_literature NP430145.RAIxq5WfdIUkCF8VF_sd8BS2BbgkmTaZAfCYB8sLr5k_4130_provenance.
- NP430145.RAIxq5WfdIUkCF8VF_sd8BS2BbgkmTaZAfCYB8sLr5k_4130_assertion SIO_000772 9743540 NP430145.RAIxq5WfdIUkCF8VF_sd8BS2BbgkmTaZAfCYB8sLr5k_4130_provenance.
- NP430145.RAIxq5WfdIUkCF8VF_sd8BS2BbgkmTaZAfCYB8sLr5k_4130_assertion wasDerivedFrom befree-20150227 NP430145.RAIxq5WfdIUkCF8VF_sd8BS2BbgkmTaZAfCYB8sLr5k_4130_provenance.
- NP430145.RAIxq5WfdIUkCF8VF_sd8BS2BbgkmTaZAfCYB8sLr5k_4130_assertion wasGeneratedBy ECO_0000203 NP430145.RAIxq5WfdIUkCF8VF_sd8BS2BbgkmTaZAfCYB8sLr5k_4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP430145.RAIxq5WfdIUkCF8VF_sd8BS2BbgkmTaZAfCYB8sLr5k_4130_provenance.