Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP246803.RAsCF5fV6r5MTtxzXIX_nvaOdFDCeEH42QQjZMMQ0iIEw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP246803.RAsCF5fV6r5MTtxzXIX_nvaOdFDCeEH42QQjZMMQ0iIEw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP246803.RAsCF5fV6r5MTtxzXIX_nvaOdFDCeEH42QQjZMMQ0iIEw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP246803.RAsCF5fV6r5MTtxzXIX_nvaOdFDCeEH42QQjZMMQ0iIEw130_provenance.
- NP246803.RAsCF5fV6r5MTtxzXIX_nvaOdFDCeEH42QQjZMMQ0iIEw130_assertion description "[Here we report a frequency of 11.2% of mutations and variants in the known Alzheimer disease genes in the dementia cohort studied and 24% in the early onset subgroup of patients, suggesting that mutations in these genes are not uncommon in Turkey and are associated with various phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP246803.RAsCF5fV6r5MTtxzXIX_nvaOdFDCeEH42QQjZMMQ0iIEw130_provenance.
- NP246803.RAsCF5fV6r5MTtxzXIX_nvaOdFDCeEH42QQjZMMQ0iIEw130_assertion evidence source_evidence_literature NP246803.RAsCF5fV6r5MTtxzXIX_nvaOdFDCeEH42QQjZMMQ0iIEw130_provenance.
- NP246803.RAsCF5fV6r5MTtxzXIX_nvaOdFDCeEH42QQjZMMQ0iIEw130_assertion SIO_000772 22503161 NP246803.RAsCF5fV6r5MTtxzXIX_nvaOdFDCeEH42QQjZMMQ0iIEw130_provenance.
- NP246803.RAsCF5fV6r5MTtxzXIX_nvaOdFDCeEH42QQjZMMQ0iIEw130_assertion wasDerivedFrom befree-20150227 NP246803.RAsCF5fV6r5MTtxzXIX_nvaOdFDCeEH42QQjZMMQ0iIEw130_provenance.
- NP246803.RAsCF5fV6r5MTtxzXIX_nvaOdFDCeEH42QQjZMMQ0iIEw130_assertion wasGeneratedBy ECO_0000203 NP246803.RAsCF5fV6r5MTtxzXIX_nvaOdFDCeEH42QQjZMMQ0iIEw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP246803.RAsCF5fV6r5MTtxzXIX_nvaOdFDCeEH42QQjZMMQ0iIEw130_provenance.