Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP318404.RAONzUy-63NaXK2TgkJ8pZjmaQ9iozfaln0g1LTRfr1sE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP318404.RAONzUy-63NaXK2TgkJ8pZjmaQ9iozfaln0g1LTRfr1sE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP318404.RAONzUy-63NaXK2TgkJ8pZjmaQ9iozfaln0g1LTRfr1sE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP318404.RAONzUy-63NaXK2TgkJ8pZjmaQ9iozfaln0g1LTRfr1sE130_provenance.
- NP318404.RAONzUy-63NaXK2TgkJ8pZjmaQ9iozfaln0g1LTRfr1sE130_assertion description "[Furthermore, we found an intronic +17G>C polymorphism in PEN2 which, in homozygous form, was greater in early onset Alzheimer's disease (EOAD) compared to controls, and one haplotype in the NCSTN gene which was linked to EOAD and familial AD (FAD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP318404.RAONzUy-63NaXK2TgkJ8pZjmaQ9iozfaln0g1LTRfr1sE130_provenance.
- NP318404.RAONzUy-63NaXK2TgkJ8pZjmaQ9iozfaln0g1LTRfr1sE130_assertion evidence source_evidence_literature NP318404.RAONzUy-63NaXK2TgkJ8pZjmaQ9iozfaln0g1LTRfr1sE130_provenance.
- NP318404.RAONzUy-63NaXK2TgkJ8pZjmaQ9iozfaln0g1LTRfr1sE130_assertion SIO_000772 16423463 NP318404.RAONzUy-63NaXK2TgkJ8pZjmaQ9iozfaln0g1LTRfr1sE130_provenance.
- NP318404.RAONzUy-63NaXK2TgkJ8pZjmaQ9iozfaln0g1LTRfr1sE130_assertion wasDerivedFrom befree-20140225 NP318404.RAONzUy-63NaXK2TgkJ8pZjmaQ9iozfaln0g1LTRfr1sE130_provenance.
- NP318404.RAONzUy-63NaXK2TgkJ8pZjmaQ9iozfaln0g1LTRfr1sE130_assertion wasGeneratedBy ECO_0000203 NP318404.RAONzUy-63NaXK2TgkJ8pZjmaQ9iozfaln0g1LTRfr1sE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP318404.RAONzUy-63NaXK2TgkJ8pZjmaQ9iozfaln0g1LTRfr1sE130_provenance.