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- source_evidence_literature type ECO_0000212 NP886752.RATbiP-82EK3b5q4mxO0xq7_-oiHpp1zhkI2vGSqeeZFM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP886752.RATbiP-82EK3b5q4mxO0xq7_-oiHpp1zhkI2vGSqeeZFM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP886752.RATbiP-82EK3b5q4mxO0xq7_-oiHpp1zhkI2vGSqeeZFM130_provenance.
- NP886752.RATbiP-82EK3b5q4mxO0xq7_-oiHpp1zhkI2vGSqeeZFM130_assertion description "[Finding of alternative associating haplotypes in the same set of BPD families gives evidence for allelic heterogeneity within DISC1, eventually leading to heterogeneity in the clinical outcome as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886752.RATbiP-82EK3b5q4mxO0xq7_-oiHpp1zhkI2vGSqeeZFM130_provenance.
- NP886752.RATbiP-82EK3b5q4mxO0xq7_-oiHpp1zhkI2vGSqeeZFM130_assertion evidence source_evidence_literature NP886752.RATbiP-82EK3b5q4mxO0xq7_-oiHpp1zhkI2vGSqeeZFM130_provenance.
- NP886752.RATbiP-82EK3b5q4mxO0xq7_-oiHpp1zhkI2vGSqeeZFM130_assertion SIO_000772 17673452 NP886752.RATbiP-82EK3b5q4mxO0xq7_-oiHpp1zhkI2vGSqeeZFM130_provenance.
- NP886752.RATbiP-82EK3b5q4mxO0xq7_-oiHpp1zhkI2vGSqeeZFM130_assertion wasDerivedFrom befree-20150227 NP886752.RATbiP-82EK3b5q4mxO0xq7_-oiHpp1zhkI2vGSqeeZFM130_provenance.
- NP886752.RATbiP-82EK3b5q4mxO0xq7_-oiHpp1zhkI2vGSqeeZFM130_assertion wasGeneratedBy ECO_0000203 NP886752.RATbiP-82EK3b5q4mxO0xq7_-oiHpp1zhkI2vGSqeeZFM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP886752.RATbiP-82EK3b5q4mxO0xq7_-oiHpp1zhkI2vGSqeeZFM130_provenance.