Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP674488.RAMnXcnOg1mClMJfaflD_75wlSCp7i_CcOvbtzSsjl2v4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP674488.RAMnXcnOg1mClMJfaflD_75wlSCp7i_CcOvbtzSsjl2v4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674488.RAMnXcnOg1mClMJfaflD_75wlSCp7i_CcOvbtzSsjl2v4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674488.RAMnXcnOg1mClMJfaflD_75wlSCp7i_CcOvbtzSsjl2v4130_provenance.
- NP674488.RAMnXcnOg1mClMJfaflD_75wlSCp7i_CcOvbtzSsjl2v4130_assertion description "[Species-specific subcellular localization of RPGR and RPGRIP isoforms: implications for the phenotypic variability of congenital retinopathies among species.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674488.RAMnXcnOg1mClMJfaflD_75wlSCp7i_CcOvbtzSsjl2v4130_provenance.
- NP674488.RAMnXcnOg1mClMJfaflD_75wlSCp7i_CcOvbtzSsjl2v4130_assertion evidence source_evidence_literature NP674488.RAMnXcnOg1mClMJfaflD_75wlSCp7i_CcOvbtzSsjl2v4130_provenance.
- NP674488.RAMnXcnOg1mClMJfaflD_75wlSCp7i_CcOvbtzSsjl2v4130_assertion SIO_000772 12140192 NP674488.RAMnXcnOg1mClMJfaflD_75wlSCp7i_CcOvbtzSsjl2v4130_provenance.
- NP674488.RAMnXcnOg1mClMJfaflD_75wlSCp7i_CcOvbtzSsjl2v4130_assertion wasDerivedFrom befree-20150227 NP674488.RAMnXcnOg1mClMJfaflD_75wlSCp7i_CcOvbtzSsjl2v4130_provenance.
- NP674488.RAMnXcnOg1mClMJfaflD_75wlSCp7i_CcOvbtzSsjl2v4130_assertion wasGeneratedBy ECO_0000203 NP674488.RAMnXcnOg1mClMJfaflD_75wlSCp7i_CcOvbtzSsjl2v4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP674488.RAMnXcnOg1mClMJfaflD_75wlSCp7i_CcOvbtzSsjl2v4130_provenance.