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- source_evidence_literature type ECO_0000212 NP832155.RAArZiv5_B7OjoyZ4PJlt6bWi_NSc4vKh4Aoq0Rc_Nx0k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP832155.RAArZiv5_B7OjoyZ4PJlt6bWi_NSc4vKh4Aoq0Rc_Nx0k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP832155.RAArZiv5_B7OjoyZ4PJlt6bWi_NSc4vKh4Aoq0Rc_Nx0k130_provenance.
- NP832155.RAArZiv5_B7OjoyZ4PJlt6bWi_NSc4vKh4Aoq0Rc_Nx0k130_assertion description "[In this report the distribution of the exonic G/A single nucleotide polymorphism (SNP) in purine nucleoside phosphorylase (PNP) gene, resulting in the amino acid substitution serine to glycine at position 51 (G51S), was investigated in a large population of AD patients (n=321) and non-demented control (n=208).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP832155.RAArZiv5_B7OjoyZ4PJlt6bWi_NSc4vKh4Aoq0Rc_Nx0k130_provenance.
- NP832155.RAArZiv5_B7OjoyZ4PJlt6bWi_NSc4vKh4Aoq0Rc_Nx0k130_assertion evidence source_evidence_literature NP832155.RAArZiv5_B7OjoyZ4PJlt6bWi_NSc4vKh4Aoq0Rc_Nx0k130_provenance.
- NP832155.RAArZiv5_B7OjoyZ4PJlt6bWi_NSc4vKh4Aoq0Rc_Nx0k130_assertion SIO_000772 17221831 NP832155.RAArZiv5_B7OjoyZ4PJlt6bWi_NSc4vKh4Aoq0Rc_Nx0k130_provenance.
- NP832155.RAArZiv5_B7OjoyZ4PJlt6bWi_NSc4vKh4Aoq0Rc_Nx0k130_assertion wasDerivedFrom befree-20140225 NP832155.RAArZiv5_B7OjoyZ4PJlt6bWi_NSc4vKh4Aoq0Rc_Nx0k130_provenance.
- NP832155.RAArZiv5_B7OjoyZ4PJlt6bWi_NSc4vKh4Aoq0Rc_Nx0k130_assertion wasGeneratedBy ECO_0000203 NP832155.RAArZiv5_B7OjoyZ4PJlt6bWi_NSc4vKh4Aoq0Rc_Nx0k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP832155.RAArZiv5_B7OjoyZ4PJlt6bWi_NSc4vKh4Aoq0Rc_Nx0k130_provenance.