Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP280764.RAt20UrzADs2YYkfiOg3CGo94VRFbPv0TxKBSF12ecivQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP280764.RAt20UrzADs2YYkfiOg3CGo94VRFbPv0TxKBSF12ecivQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP280764.RAt20UrzADs2YYkfiOg3CGo94VRFbPv0TxKBSF12ecivQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP280764.RAt20UrzADs2YYkfiOg3CGo94VRFbPv0TxKBSF12ecivQ130_provenance.
- NP280764.RAt20UrzADs2YYkfiOg3CGo94VRFbPv0TxKBSF12ecivQ130_assertion description "[The deleted region contained the SEZ6L (Seizure 6-like) gene, whose structure had been partially determined by the chromosome 22 sequencing project.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280764.RAt20UrzADs2YYkfiOg3CGo94VRFbPv0TxKBSF12ecivQ130_provenance.
- NP280764.RAt20UrzADs2YYkfiOg3CGo94VRFbPv0TxKBSF12ecivQ130_assertion evidence source_evidence_literature NP280764.RAt20UrzADs2YYkfiOg3CGo94VRFbPv0TxKBSF12ecivQ130_provenance.
- NP280764.RAt20UrzADs2YYkfiOg3CGo94VRFbPv0TxKBSF12ecivQ130_assertion SIO_000772 11175339 NP280764.RAt20UrzADs2YYkfiOg3CGo94VRFbPv0TxKBSF12ecivQ130_provenance.
- NP280764.RAt20UrzADs2YYkfiOg3CGo94VRFbPv0TxKBSF12ecivQ130_assertion wasDerivedFrom befree-20140225 NP280764.RAt20UrzADs2YYkfiOg3CGo94VRFbPv0TxKBSF12ecivQ130_provenance.
- NP280764.RAt20UrzADs2YYkfiOg3CGo94VRFbPv0TxKBSF12ecivQ130_assertion wasGeneratedBy ECO_0000203 NP280764.RAt20UrzADs2YYkfiOg3CGo94VRFbPv0TxKBSF12ecivQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP280764.RAt20UrzADs2YYkfiOg3CGo94VRFbPv0TxKBSF12ecivQ130_provenance.