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- source_evidence_literature type ECO_0000212 NP806226.RAcL9wbgkuDtR7uea-HA4GFJZXgbgYge1uZEoxZBOG2bI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP806226.RAcL9wbgkuDtR7uea-HA4GFJZXgbgYge1uZEoxZBOG2bI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP806226.RAcL9wbgkuDtR7uea-HA4GFJZXgbgYge1uZEoxZBOG2bI130_provenance.
- NP806226.RAcL9wbgkuDtR7uea-HA4GFJZXgbgYge1uZEoxZBOG2bI130_assertion description "[Wagner syndrome (WGN1) is associated with mutations in versican (CSPG2) and snowflake vitreoretinal degeneration (SVD) with a mutation in a potassium channel (KCNJ13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806226.RAcL9wbgkuDtR7uea-HA4GFJZXgbgYge1uZEoxZBOG2bI130_provenance.
- NP806226.RAcL9wbgkuDtR7uea-HA4GFJZXgbgYge1uZEoxZBOG2bI130_assertion evidence source_evidence_literature NP806226.RAcL9wbgkuDtR7uea-HA4GFJZXgbgYge1uZEoxZBOG2bI130_provenance.
- NP806226.RAcL9wbgkuDtR7uea-HA4GFJZXgbgYge1uZEoxZBOG2bI130_assertion SIO_000772 18309337 NP806226.RAcL9wbgkuDtR7uea-HA4GFJZXgbgYge1uZEoxZBOG2bI130_provenance.
- NP806226.RAcL9wbgkuDtR7uea-HA4GFJZXgbgYge1uZEoxZBOG2bI130_assertion wasDerivedFrom befree-20140225 NP806226.RAcL9wbgkuDtR7uea-HA4GFJZXgbgYge1uZEoxZBOG2bI130_provenance.
- NP806226.RAcL9wbgkuDtR7uea-HA4GFJZXgbgYge1uZEoxZBOG2bI130_assertion wasGeneratedBy ECO_0000203 NP806226.RAcL9wbgkuDtR7uea-HA4GFJZXgbgYge1uZEoxZBOG2bI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP806226.RAcL9wbgkuDtR7uea-HA4GFJZXgbgYge1uZEoxZBOG2bI130_provenance.