Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP936466.RAN-mDCeshkblqxKyhIRn-7j2UmRPty9_nDs5sqjZYwjU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP936466.RAN-mDCeshkblqxKyhIRn-7j2UmRPty9_nDs5sqjZYwjU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936466.RAN-mDCeshkblqxKyhIRn-7j2UmRPty9_nDs5sqjZYwjU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936466.RAN-mDCeshkblqxKyhIRn-7j2UmRPty9_nDs5sqjZYwjU130_provenance.
- NP936466.RAN-mDCeshkblqxKyhIRn-7j2UmRPty9_nDs5sqjZYwjU130_assertion description "[The altered expression of IGF2 has been implicated in Beckwith-Wiedemann syndrome, a human fetal overgrowth syndrome, which is characterized by overgrowth of several organs and an increased risk of developing childhood tumours.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936466.RAN-mDCeshkblqxKyhIRn-7j2UmRPty9_nDs5sqjZYwjU130_provenance.
- NP936466.RAN-mDCeshkblqxKyhIRn-7j2UmRPty9_nDs5sqjZYwjU130_assertion evidence source_evidence_literature NP936466.RAN-mDCeshkblqxKyhIRn-7j2UmRPty9_nDs5sqjZYwjU130_provenance.
- NP936466.RAN-mDCeshkblqxKyhIRn-7j2UmRPty9_nDs5sqjZYwjU130_assertion SIO_000772 9349812 NP936466.RAN-mDCeshkblqxKyhIRn-7j2UmRPty9_nDs5sqjZYwjU130_provenance.
- NP936466.RAN-mDCeshkblqxKyhIRn-7j2UmRPty9_nDs5sqjZYwjU130_assertion wasDerivedFrom befree-20140225 NP936466.RAN-mDCeshkblqxKyhIRn-7j2UmRPty9_nDs5sqjZYwjU130_provenance.
- NP936466.RAN-mDCeshkblqxKyhIRn-7j2UmRPty9_nDs5sqjZYwjU130_assertion wasGeneratedBy ECO_0000203 NP936466.RAN-mDCeshkblqxKyhIRn-7j2UmRPty9_nDs5sqjZYwjU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP936466.RAN-mDCeshkblqxKyhIRn-7j2UmRPty9_nDs5sqjZYwjU130_provenance.