Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP782454.RAYFvFE7jWXwjUhiNlUwgzCpk4B1bVmlMVpsm6uW1ktYk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP782454.RAYFvFE7jWXwjUhiNlUwgzCpk4B1bVmlMVpsm6uW1ktYk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP782454.RAYFvFE7jWXwjUhiNlUwgzCpk4B1bVmlMVpsm6uW1ktYk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP782454.RAYFvFE7jWXwjUhiNlUwgzCpk4B1bVmlMVpsm6uW1ktYk130_provenance.
- NP782454.RAYFvFE7jWXwjUhiNlUwgzCpk4B1bVmlMVpsm6uW1ktYk130_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." NP782454.RAYFvFE7jWXwjUhiNlUwgzCpk4B1bVmlMVpsm6uW1ktYk130_provenance.
- NP782454.RAYFvFE7jWXwjUhiNlUwgzCpk4B1bVmlMVpsm6uW1ktYk130_assertion evidence source_evidence_literature NP782454.RAYFvFE7jWXwjUhiNlUwgzCpk4B1bVmlMVpsm6uW1ktYk130_provenance.
- NP782454.RAYFvFE7jWXwjUhiNlUwgzCpk4B1bVmlMVpsm6uW1ktYk130_assertion SIO_000772 24123890 NP782454.RAYFvFE7jWXwjUhiNlUwgzCpk4B1bVmlMVpsm6uW1ktYk130_provenance.
- NP782454.RAYFvFE7jWXwjUhiNlUwgzCpk4B1bVmlMVpsm6uW1ktYk130_assertion wasDerivedFrom befree-20150227 NP782454.RAYFvFE7jWXwjUhiNlUwgzCpk4B1bVmlMVpsm6uW1ktYk130_provenance.
- NP782454.RAYFvFE7jWXwjUhiNlUwgzCpk4B1bVmlMVpsm6uW1ktYk130_assertion wasGeneratedBy ECO_0000203 NP782454.RAYFvFE7jWXwjUhiNlUwgzCpk4B1bVmlMVpsm6uW1ktYk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP782454.RAYFvFE7jWXwjUhiNlUwgzCpk4B1bVmlMVpsm6uW1ktYk130_provenance.