Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP712032.RA5NX5ul9_TYSL53NA4IMwbDwLdBEkLEsrfOaVQB1BtBY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP712032.RA5NX5ul9_TYSL53NA4IMwbDwLdBEkLEsrfOaVQB1BtBY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP712032.RA5NX5ul9_TYSL53NA4IMwbDwLdBEkLEsrfOaVQB1BtBY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP712032.RA5NX5ul9_TYSL53NA4IMwbDwLdBEkLEsrfOaVQB1BtBY130_provenance.
- NP712032.RA5NX5ul9_TYSL53NA4IMwbDwLdBEkLEsrfOaVQB1BtBY130_assertion description "[Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP712032.RA5NX5ul9_TYSL53NA4IMwbDwLdBEkLEsrfOaVQB1BtBY130_provenance.
- NP712032.RA5NX5ul9_TYSL53NA4IMwbDwLdBEkLEsrfOaVQB1BtBY130_assertion evidence source_evidence_literature NP712032.RA5NX5ul9_TYSL53NA4IMwbDwLdBEkLEsrfOaVQB1BtBY130_provenance.
- NP712032.RA5NX5ul9_TYSL53NA4IMwbDwLdBEkLEsrfOaVQB1BtBY130_assertion SIO_000772 22312439 NP712032.RA5NX5ul9_TYSL53NA4IMwbDwLdBEkLEsrfOaVQB1BtBY130_provenance.
- NP712032.RA5NX5ul9_TYSL53NA4IMwbDwLdBEkLEsrfOaVQB1BtBY130_assertion wasDerivedFrom befree-20140225 NP712032.RA5NX5ul9_TYSL53NA4IMwbDwLdBEkLEsrfOaVQB1BtBY130_provenance.
- NP712032.RA5NX5ul9_TYSL53NA4IMwbDwLdBEkLEsrfOaVQB1BtBY130_assertion wasGeneratedBy ECO_0000203 NP712032.RA5NX5ul9_TYSL53NA4IMwbDwLdBEkLEsrfOaVQB1BtBY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP712032.RA5NX5ul9_TYSL53NA4IMwbDwLdBEkLEsrfOaVQB1BtBY130_provenance.