Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP420802.RAVmkGt-pq5LSbJ8KJXM_iW-bLc7grsz3jjP4hpR0Q-U4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP420802.RAVmkGt-pq5LSbJ8KJXM_iW-bLc7grsz3jjP4hpR0Q-U4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420802.RAVmkGt-pq5LSbJ8KJXM_iW-bLc7grsz3jjP4hpR0Q-U4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420802.RAVmkGt-pq5LSbJ8KJXM_iW-bLc7grsz3jjP4hpR0Q-U4130_provenance.
- NP420802.RAVmkGt-pq5LSbJ8KJXM_iW-bLc7grsz3jjP4hpR0Q-U4130_assertion description "[Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420802.RAVmkGt-pq5LSbJ8KJXM_iW-bLc7grsz3jjP4hpR0Q-U4130_provenance.
- NP420802.RAVmkGt-pq5LSbJ8KJXM_iW-bLc7grsz3jjP4hpR0Q-U4130_assertion evidence source_evidence_literature NP420802.RAVmkGt-pq5LSbJ8KJXM_iW-bLc7grsz3jjP4hpR0Q-U4130_provenance.
- NP420802.RAVmkGt-pq5LSbJ8KJXM_iW-bLc7grsz3jjP4hpR0Q-U4130_assertion SIO_000772 23759358 NP420802.RAVmkGt-pq5LSbJ8KJXM_iW-bLc7grsz3jjP4hpR0Q-U4130_provenance.
- NP420802.RAVmkGt-pq5LSbJ8KJXM_iW-bLc7grsz3jjP4hpR0Q-U4130_assertion wasDerivedFrom befree-20140225 NP420802.RAVmkGt-pq5LSbJ8KJXM_iW-bLc7grsz3jjP4hpR0Q-U4130_provenance.
- NP420802.RAVmkGt-pq5LSbJ8KJXM_iW-bLc7grsz3jjP4hpR0Q-U4130_assertion wasGeneratedBy ECO_0000203 NP420802.RAVmkGt-pq5LSbJ8KJXM_iW-bLc7grsz3jjP4hpR0Q-U4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP420802.RAVmkGt-pq5LSbJ8KJXM_iW-bLc7grsz3jjP4hpR0Q-U4130_provenance.