Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP933096.RA81973oI8rn7pelZ20Uw9VubSh7TxSM-E_Lie2H5_E_I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP933096.RA81973oI8rn7pelZ20Uw9VubSh7TxSM-E_Lie2H5_E_I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP933096.RA81973oI8rn7pelZ20Uw9VubSh7TxSM-E_Lie2H5_E_I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP933096.RA81973oI8rn7pelZ20Uw9VubSh7TxSM-E_Lie2H5_E_I130_provenance.
- NP933096.RA81973oI8rn7pelZ20Uw9VubSh7TxSM-E_Lie2H5_E_I130_assertion description "[It further suggests that WDR19 mutations can cause a broad spectrum of ciliopathies that extends to Jeune and Sensenbrenner syndromes, RP and renal NPHP-like phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP933096.RA81973oI8rn7pelZ20Uw9VubSh7TxSM-E_Lie2H5_E_I130_provenance.
- NP933096.RA81973oI8rn7pelZ20Uw9VubSh7TxSM-E_Lie2H5_E_I130_assertion evidence source_evidence_literature NP933096.RA81973oI8rn7pelZ20Uw9VubSh7TxSM-E_Lie2H5_E_I130_provenance.
- NP933096.RA81973oI8rn7pelZ20Uw9VubSh7TxSM-E_Lie2H5_E_I130_assertion SIO_000772 24504730 NP933096.RA81973oI8rn7pelZ20Uw9VubSh7TxSM-E_Lie2H5_E_I130_provenance.
- NP933096.RA81973oI8rn7pelZ20Uw9VubSh7TxSM-E_Lie2H5_E_I130_assertion wasDerivedFrom befree-20150227 NP933096.RA81973oI8rn7pelZ20Uw9VubSh7TxSM-E_Lie2H5_E_I130_provenance.
- NP933096.RA81973oI8rn7pelZ20Uw9VubSh7TxSM-E_Lie2H5_E_I130_assertion wasGeneratedBy ECO_0000203 NP933096.RA81973oI8rn7pelZ20Uw9VubSh7TxSM-E_Lie2H5_E_I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP933096.RA81973oI8rn7pelZ20Uw9VubSh7TxSM-E_Lie2H5_E_I130_provenance.