Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978059.RAJrmdl_po4p_qAEdyCc7RQ4g8nhBxVf2BLxKmnNFIFIU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978059.RAJrmdl_po4p_qAEdyCc7RQ4g8nhBxVf2BLxKmnNFIFIU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978059.RAJrmdl_po4p_qAEdyCc7RQ4g8nhBxVf2BLxKmnNFIFIU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978059.RAJrmdl_po4p_qAEdyCc7RQ4g8nhBxVf2BLxKmnNFIFIU130_provenance.
- NP978059.RAJrmdl_po4p_qAEdyCc7RQ4g8nhBxVf2BLxKmnNFIFIU130_assertion description "[In humans, a mutation in the Glis2 gene has been linked to the development of nephronophthisis (NPHP), a recessive cystic kidney disease, while mutations in Glis3 lead to an extended multisystem phenotype that includes the development of neonatal diabetes, polycystic kidneys, congenital hypothyroidism, and facial dysmorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978059.RAJrmdl_po4p_qAEdyCc7RQ4g8nhBxVf2BLxKmnNFIFIU130_provenance.
- NP978059.RAJrmdl_po4p_qAEdyCc7RQ4g8nhBxVf2BLxKmnNFIFIU130_assertion evidence source_evidence_literature NP978059.RAJrmdl_po4p_qAEdyCc7RQ4g8nhBxVf2BLxKmnNFIFIU130_provenance.
- NP978059.RAJrmdl_po4p_qAEdyCc7RQ4g8nhBxVf2BLxKmnNFIFIU130_assertion SIO_000772 22391303 NP978059.RAJrmdl_po4p_qAEdyCc7RQ4g8nhBxVf2BLxKmnNFIFIU130_provenance.
- NP978059.RAJrmdl_po4p_qAEdyCc7RQ4g8nhBxVf2BLxKmnNFIFIU130_assertion wasDerivedFrom befree-20150227 NP978059.RAJrmdl_po4p_qAEdyCc7RQ4g8nhBxVf2BLxKmnNFIFIU130_provenance.
- NP978059.RAJrmdl_po4p_qAEdyCc7RQ4g8nhBxVf2BLxKmnNFIFIU130_assertion wasGeneratedBy ECO_0000203 NP978059.RAJrmdl_po4p_qAEdyCc7RQ4g8nhBxVf2BLxKmnNFIFIU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978059.RAJrmdl_po4p_qAEdyCc7RQ4g8nhBxVf2BLxKmnNFIFIU130_provenance.