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- source_evidence_literature type ECO_0000212 NP370565.RAicsL9QZpkvhgfaMm-zl1ai7lMh5oFAYmptFcodOqOSM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP370565.RAicsL9QZpkvhgfaMm-zl1ai7lMh5oFAYmptFcodOqOSM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP370565.RAicsL9QZpkvhgfaMm-zl1ai7lMh5oFAYmptFcodOqOSM130_provenance.
- NP370565.RAicsL9QZpkvhgfaMm-zl1ai7lMh5oFAYmptFcodOqOSM130_assertion description "[It is well-established that the APOE ?4 allele and homozygosity at polymorphic codon 129 in the PRNP gene are the major genetic risk factors for AD and human prion diseases, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP370565.RAicsL9QZpkvhgfaMm-zl1ai7lMh5oFAYmptFcodOqOSM130_provenance.
- NP370565.RAicsL9QZpkvhgfaMm-zl1ai7lMh5oFAYmptFcodOqOSM130_assertion evidence source_evidence_literature NP370565.RAicsL9QZpkvhgfaMm-zl1ai7lMh5oFAYmptFcodOqOSM130_provenance.
- NP370565.RAicsL9QZpkvhgfaMm-zl1ai7lMh5oFAYmptFcodOqOSM130_assertion SIO_000772 21799773 NP370565.RAicsL9QZpkvhgfaMm-zl1ai7lMh5oFAYmptFcodOqOSM130_provenance.
- NP370565.RAicsL9QZpkvhgfaMm-zl1ai7lMh5oFAYmptFcodOqOSM130_assertion wasDerivedFrom befree-20140225 NP370565.RAicsL9QZpkvhgfaMm-zl1ai7lMh5oFAYmptFcodOqOSM130_provenance.
- NP370565.RAicsL9QZpkvhgfaMm-zl1ai7lMh5oFAYmptFcodOqOSM130_assertion wasGeneratedBy ECO_0000203 NP370565.RAicsL9QZpkvhgfaMm-zl1ai7lMh5oFAYmptFcodOqOSM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP370565.RAicsL9QZpkvhgfaMm-zl1ai7lMh5oFAYmptFcodOqOSM130_provenance.