Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP554546.RAxXSWMnWnT_6uuS-nngLLgU9g3_CCGhszwoH6_AkkqH8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP554546.RAxXSWMnWnT_6uuS-nngLLgU9g3_CCGhszwoH6_AkkqH8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP554546.RAxXSWMnWnT_6uuS-nngLLgU9g3_CCGhszwoH6_AkkqH8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP554546.RAxXSWMnWnT_6uuS-nngLLgU9g3_CCGhszwoH6_AkkqH8130_provenance.
- NP554546.RAxXSWMnWnT_6uuS-nngLLgU9g3_CCGhszwoH6_AkkqH8130_assertion wasGeneratedBy ECO_0000203 NP554546.RAxXSWMnWnT_6uuS-nngLLgU9g3_CCGhszwoH6_AkkqH8130_provenance.
- NP554546.RAxXSWMnWnT_6uuS-nngLLgU9g3_CCGhszwoH6_AkkqH8130_assertion wasDerivedFrom befree-20140225 NP554546.RAxXSWMnWnT_6uuS-nngLLgU9g3_CCGhszwoH6_AkkqH8130_provenance.
- NP554546.RAxXSWMnWnT_6uuS-nngLLgU9g3_CCGhszwoH6_AkkqH8130_assertion SIO_000772 11496370 NP554546.RAxXSWMnWnT_6uuS-nngLLgU9g3_CCGhszwoH6_AkkqH8130_provenance.
- NP554546.RAxXSWMnWnT_6uuS-nngLLgU9g3_CCGhszwoH6_AkkqH8130_assertion evidence source_evidence_literature NP554546.RAxXSWMnWnT_6uuS-nngLLgU9g3_CCGhszwoH6_AkkqH8130_provenance.
- NP554546.RAxXSWMnWnT_6uuS-nngLLgU9g3_CCGhszwoH6_AkkqH8130_assertion description "[The results are supportive of UFD1L involvement in the neurodevelopmental origin of schizophrenia and contribute in delineating etiological and pathogenetic mechanism of the schizophrenia subtype related to 22q11.2 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP554546.RAxXSWMnWnT_6uuS-nngLLgU9g3_CCGhszwoH6_AkkqH8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP554546.RAxXSWMnWnT_6uuS-nngLLgU9g3_CCGhszwoH6_AkkqH8130_provenance.