Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP216109.RAFjlBWt6KEK0yEUftMmXy4D2G1iOdR9N_vpzgGSkLEcM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP216109.RAFjlBWt6KEK0yEUftMmXy4D2G1iOdR9N_vpzgGSkLEcM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP216109.RAFjlBWt6KEK0yEUftMmXy4D2G1iOdR9N_vpzgGSkLEcM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP216109.RAFjlBWt6KEK0yEUftMmXy4D2G1iOdR9N_vpzgGSkLEcM130_provenance.
- NP216109.RAFjlBWt6KEK0yEUftMmXy4D2G1iOdR9N_vpzgGSkLEcM130_assertion description "[Pathogenic mutations in APP, PSEN1, PSEN2, MAPT and GRN have previously been linked to familial early onset forms of dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216109.RAFjlBWt6KEK0yEUftMmXy4D2G1iOdR9N_vpzgGSkLEcM130_provenance.
- NP216109.RAFjlBWt6KEK0yEUftMmXy4D2G1iOdR9N_vpzgGSkLEcM130_assertion evidence source_evidence_literature NP216109.RAFjlBWt6KEK0yEUftMmXy4D2G1iOdR9N_vpzgGSkLEcM130_provenance.
- NP216109.RAFjlBWt6KEK0yEUftMmXy4D2G1iOdR9N_vpzgGSkLEcM130_assertion SIO_000772 22312439 NP216109.RAFjlBWt6KEK0yEUftMmXy4D2G1iOdR9N_vpzgGSkLEcM130_provenance.
- NP216109.RAFjlBWt6KEK0yEUftMmXy4D2G1iOdR9N_vpzgGSkLEcM130_assertion wasDerivedFrom befree-20140225 NP216109.RAFjlBWt6KEK0yEUftMmXy4D2G1iOdR9N_vpzgGSkLEcM130_provenance.
- NP216109.RAFjlBWt6KEK0yEUftMmXy4D2G1iOdR9N_vpzgGSkLEcM130_assertion wasGeneratedBy ECO_0000203 NP216109.RAFjlBWt6KEK0yEUftMmXy4D2G1iOdR9N_vpzgGSkLEcM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP216109.RAFjlBWt6KEK0yEUftMmXy4D2G1iOdR9N_vpzgGSkLEcM130_provenance.