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- source_evidence_literature type ECO_0000212 NP1119017.RAOhr2nZ9JUtzBD0qEdXF3R-SMT7jqi6mRrQv4LMsJHS0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1119017.RAOhr2nZ9JUtzBD0qEdXF3R-SMT7jqi6mRrQv4LMsJHS0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1119017.RAOhr2nZ9JUtzBD0qEdXF3R-SMT7jqi6mRrQv4LMsJHS0130_provenance.
- NP1119017.RAOhr2nZ9JUtzBD0qEdXF3R-SMT7jqi6mRrQv4LMsJHS0130_assertion description "[Here we report ZIC3 sequencing results from 440 unrelated patients with heterotaxy and CHD, the largest cohort yet examined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1119017.RAOhr2nZ9JUtzBD0qEdXF3R-SMT7jqi6mRrQv4LMsJHS0130_provenance.
- NP1119017.RAOhr2nZ9JUtzBD0qEdXF3R-SMT7jqi6mRrQv4LMsJHS0130_assertion evidence source_evidence_literature NP1119017.RAOhr2nZ9JUtzBD0qEdXF3R-SMT7jqi6mRrQv4LMsJHS0130_provenance.
- NP1119017.RAOhr2nZ9JUtzBD0qEdXF3R-SMT7jqi6mRrQv4LMsJHS0130_assertion SIO_000772 24123890 NP1119017.RAOhr2nZ9JUtzBD0qEdXF3R-SMT7jqi6mRrQv4LMsJHS0130_provenance.
- NP1119017.RAOhr2nZ9JUtzBD0qEdXF3R-SMT7jqi6mRrQv4LMsJHS0130_assertion wasDerivedFrom befree-2016 NP1119017.RAOhr2nZ9JUtzBD0qEdXF3R-SMT7jqi6mRrQv4LMsJHS0130_provenance.
- NP1119017.RAOhr2nZ9JUtzBD0qEdXF3R-SMT7jqi6mRrQv4LMsJHS0130_assertion wasGeneratedBy ECO_0000203 NP1119017.RAOhr2nZ9JUtzBD0qEdXF3R-SMT7jqi6mRrQv4LMsJHS0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1119017.RAOhr2nZ9JUtzBD0qEdXF3R-SMT7jqi6mRrQv4LMsJHS0130_provenance.