Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP419529.RAH_O80Tv8hVyfQYpPXY_TEyNQi7a8HFXtdeX8bCp-h-I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP419529.RAH_O80Tv8hVyfQYpPXY_TEyNQi7a8HFXtdeX8bCp-h-I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP419529.RAH_O80Tv8hVyfQYpPXY_TEyNQi7a8HFXtdeX8bCp-h-I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP419529.RAH_O80Tv8hVyfQYpPXY_TEyNQi7a8HFXtdeX8bCp-h-I130_provenance.
- NP419529.RAH_O80Tv8hVyfQYpPXY_TEyNQi7a8HFXtdeX8bCp-h-I130_assertion description "[Mutations in GATA4 have been related to human congenital heart diseases (CHDs) in several studies, whereas mutations in GATA6 have only recently been reported in patients with persistent truncus arteriosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419529.RAH_O80Tv8hVyfQYpPXY_TEyNQi7a8HFXtdeX8bCp-h-I130_provenance.
- NP419529.RAH_O80Tv8hVyfQYpPXY_TEyNQi7a8HFXtdeX8bCp-h-I130_assertion evidence source_evidence_literature NP419529.RAH_O80Tv8hVyfQYpPXY_TEyNQi7a8HFXtdeX8bCp-h-I130_provenance.
- NP419529.RAH_O80Tv8hVyfQYpPXY_TEyNQi7a8HFXtdeX8bCp-h-I130_assertion SIO_000772 20631719 NP419529.RAH_O80Tv8hVyfQYpPXY_TEyNQi7a8HFXtdeX8bCp-h-I130_provenance.
- NP419529.RAH_O80Tv8hVyfQYpPXY_TEyNQi7a8HFXtdeX8bCp-h-I130_assertion wasDerivedFrom befree-20150227 NP419529.RAH_O80Tv8hVyfQYpPXY_TEyNQi7a8HFXtdeX8bCp-h-I130_provenance.
- NP419529.RAH_O80Tv8hVyfQYpPXY_TEyNQi7a8HFXtdeX8bCp-h-I130_assertion wasGeneratedBy ECO_0000203 NP419529.RAH_O80Tv8hVyfQYpPXY_TEyNQi7a8HFXtdeX8bCp-h-I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP419529.RAH_O80Tv8hVyfQYpPXY_TEyNQi7a8HFXtdeX8bCp-h-I130_provenance.