Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP616415.RAUsiPkeyZZh391eeNfuL_fElRk9rTE4fM_T4CDSYhIAU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP616415.RAUsiPkeyZZh391eeNfuL_fElRk9rTE4fM_T4CDSYhIAU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616415.RAUsiPkeyZZh391eeNfuL_fElRk9rTE4fM_T4CDSYhIAU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616415.RAUsiPkeyZZh391eeNfuL_fElRk9rTE4fM_T4CDSYhIAU130_provenance.
- NP616415.RAUsiPkeyZZh391eeNfuL_fElRk9rTE4fM_T4CDSYhIAU130_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." NP616415.RAUsiPkeyZZh391eeNfuL_fElRk9rTE4fM_T4CDSYhIAU130_provenance.
- NP616415.RAUsiPkeyZZh391eeNfuL_fElRk9rTE4fM_T4CDSYhIAU130_assertion evidence source_evidence_literature NP616415.RAUsiPkeyZZh391eeNfuL_fElRk9rTE4fM_T4CDSYhIAU130_provenance.
- NP616415.RAUsiPkeyZZh391eeNfuL_fElRk9rTE4fM_T4CDSYhIAU130_assertion SIO_000772 20631719 NP616415.RAUsiPkeyZZh391eeNfuL_fElRk9rTE4fM_T4CDSYhIAU130_provenance.
- NP616415.RAUsiPkeyZZh391eeNfuL_fElRk9rTE4fM_T4CDSYhIAU130_assertion wasDerivedFrom befree-20140225 NP616415.RAUsiPkeyZZh391eeNfuL_fElRk9rTE4fM_T4CDSYhIAU130_provenance.
- NP616415.RAUsiPkeyZZh391eeNfuL_fElRk9rTE4fM_T4CDSYhIAU130_assertion wasGeneratedBy ECO_0000203 NP616415.RAUsiPkeyZZh391eeNfuL_fElRk9rTE4fM_T4CDSYhIAU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP616415.RAUsiPkeyZZh391eeNfuL_fElRk9rTE4fM_T4CDSYhIAU130_provenance.