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- source_evidence_literature type ECO_0000212 NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_provenance.
- NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_assertion description "[PCDH21 mutations are not a major cause of the retinal diseases investigated herein, and the corresponding human phenotype remains to be determined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_provenance.
- NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_assertion evidence source_evidence_literature NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_provenance.
- NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_assertion SIO_000772 16288196 NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_provenance.
- NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_assertion wasDerivedFrom befree-20150227 NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_provenance.
- NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_assertion wasGeneratedBy ECO_0000203 NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_provenance.