Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1246784.RANHuD_RVZpuWX5iYwg2T3Hbucil_pbhFmeEhGrcd_oQ4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1246784.RANHuD_RVZpuWX5iYwg2T3Hbucil_pbhFmeEhGrcd_oQ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246784.RANHuD_RVZpuWX5iYwg2T3Hbucil_pbhFmeEhGrcd_oQ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246784.RANHuD_RVZpuWX5iYwg2T3Hbucil_pbhFmeEhGrcd_oQ4130_provenance.
- NP1246784.RANHuD_RVZpuWX5iYwg2T3Hbucil_pbhFmeEhGrcd_oQ4130_assertion description "[Incidence of dementia in relation to genetic variants at PITX2, ZFHX3, and ApoE ?4 in atrial fibrillation patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246784.RANHuD_RVZpuWX5iYwg2T3Hbucil_pbhFmeEhGrcd_oQ4130_provenance.
- NP1246784.RANHuD_RVZpuWX5iYwg2T3Hbucil_pbhFmeEhGrcd_oQ4130_assertion evidence source_evidence_literature NP1246784.RANHuD_RVZpuWX5iYwg2T3Hbucil_pbhFmeEhGrcd_oQ4130_provenance.
- NP1246784.RANHuD_RVZpuWX5iYwg2T3Hbucil_pbhFmeEhGrcd_oQ4130_assertion SIO_000772 25494715 NP1246784.RANHuD_RVZpuWX5iYwg2T3Hbucil_pbhFmeEhGrcd_oQ4130_provenance.
- NP1246784.RANHuD_RVZpuWX5iYwg2T3Hbucil_pbhFmeEhGrcd_oQ4130_assertion wasDerivedFrom befree-2016 NP1246784.RANHuD_RVZpuWX5iYwg2T3Hbucil_pbhFmeEhGrcd_oQ4130_provenance.
- NP1246784.RANHuD_RVZpuWX5iYwg2T3Hbucil_pbhFmeEhGrcd_oQ4130_assertion wasGeneratedBy ECO_0000203 NP1246784.RANHuD_RVZpuWX5iYwg2T3Hbucil_pbhFmeEhGrcd_oQ4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246784.RANHuD_RVZpuWX5iYwg2T3Hbucil_pbhFmeEhGrcd_oQ4130_provenance.