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- source_evidence_literature type ECO_0000212 NP94442.RA6Tnw73c6fyPtU_4lAHsfKED4iZj1nnxgC-btEHmDwQk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP94442.RA6Tnw73c6fyPtU_4lAHsfKED4iZj1nnxgC-btEHmDwQk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP94442.RA6Tnw73c6fyPtU_4lAHsfKED4iZj1nnxgC-btEHmDwQk130_provenance.
- NP94442.RA6Tnw73c6fyPtU_4lAHsfKED4iZj1nnxgC-btEHmDwQk130_assertion description "[The small effect sizes may limit the prognostic, diagnostic, and therapeutic use of SNP markers such as those in MAMDC1. However, the present study demonstrates the potential of a GWAS to discover potentially important pathogenic pathways for which clinically more powerful (bio)markers may eventually be developed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94442.RA6Tnw73c6fyPtU_4lAHsfKED4iZj1nnxgC-btEHmDwQk130_provenance.
- NP94442.RA6Tnw73c6fyPtU_4lAHsfKED4iZj1nnxgC-btEHmDwQk130_assertion evidence source_evidence_literature NP94442.RA6Tnw73c6fyPtU_4lAHsfKED4iZj1nnxgC-btEHmDwQk130_provenance.
- NP94442.RA6Tnw73c6fyPtU_4lAHsfKED4iZj1nnxgC-btEHmDwQk130_assertion SIO_000772 18762592 NP94442.RA6Tnw73c6fyPtU_4lAHsfKED4iZj1nnxgC-btEHmDwQk130_provenance.
- NP94442.RA6Tnw73c6fyPtU_4lAHsfKED4iZj1nnxgC-btEHmDwQk130_assertion wasDerivedFrom gad-20130706 NP94442.RA6Tnw73c6fyPtU_4lAHsfKED4iZj1nnxgC-btEHmDwQk130_provenance.
- NP94442.RA6Tnw73c6fyPtU_4lAHsfKED4iZj1nnxgC-btEHmDwQk130_assertion wasGeneratedBy ECO_0000203 NP94442.RA6Tnw73c6fyPtU_4lAHsfKED4iZj1nnxgC-btEHmDwQk130_provenance.
- gad-20130706 importedOn "2013-07-06" NP94442.RA6Tnw73c6fyPtU_4lAHsfKED4iZj1nnxgC-btEHmDwQk130_provenance.