Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP955766.RAlYAYtrfQ_3FE-1QdD_RRXSYcCDOUgvEeMeN76NEYhLY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP955766.RAlYAYtrfQ_3FE-1QdD_RRXSYcCDOUgvEeMeN76NEYhLY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP955766.RAlYAYtrfQ_3FE-1QdD_RRXSYcCDOUgvEeMeN76NEYhLY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP955766.RAlYAYtrfQ_3FE-1QdD_RRXSYcCDOUgvEeMeN76NEYhLY130_provenance.
- NP955766.RAlYAYtrfQ_3FE-1QdD_RRXSYcCDOUgvEeMeN76NEYhLY130_assertion description "[This study points to the involvement of several genes (particularly RNF135 and CENTA2) in the increased risk of malignancy observed in NF1-microdeleted patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP955766.RAlYAYtrfQ_3FE-1QdD_RRXSYcCDOUgvEeMeN76NEYhLY130_provenance.
- NP955766.RAlYAYtrfQ_3FE-1QdD_RRXSYcCDOUgvEeMeN76NEYhLY130_assertion evidence source_evidence_literature NP955766.RAlYAYtrfQ_3FE-1QdD_RRXSYcCDOUgvEeMeN76NEYhLY130_provenance.
- NP955766.RAlYAYtrfQ_3FE-1QdD_RRXSYcCDOUgvEeMeN76NEYhLY130_assertion SIO_000772 20844836 NP955766.RAlYAYtrfQ_3FE-1QdD_RRXSYcCDOUgvEeMeN76NEYhLY130_provenance.
- NP955766.RAlYAYtrfQ_3FE-1QdD_RRXSYcCDOUgvEeMeN76NEYhLY130_assertion wasDerivedFrom befree-20150227 NP955766.RAlYAYtrfQ_3FE-1QdD_RRXSYcCDOUgvEeMeN76NEYhLY130_provenance.
- NP955766.RAlYAYtrfQ_3FE-1QdD_RRXSYcCDOUgvEeMeN76NEYhLY130_assertion wasGeneratedBy ECO_0000203 NP955766.RAlYAYtrfQ_3FE-1QdD_RRXSYcCDOUgvEeMeN76NEYhLY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP955766.RAlYAYtrfQ_3FE-1QdD_RRXSYcCDOUgvEeMeN76NEYhLY130_provenance.