Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1249428.RAYEArGLeoLwEW75ceonJ8GR16O7j86DZfV4Ts1fwT3Jk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1249428.RAYEArGLeoLwEW75ceonJ8GR16O7j86DZfV4Ts1fwT3Jk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1249428.RAYEArGLeoLwEW75ceonJ8GR16O7j86DZfV4Ts1fwT3Jk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1249428.RAYEArGLeoLwEW75ceonJ8GR16O7j86DZfV4Ts1fwT3Jk130_provenance.
- NP1249428.RAYEArGLeoLwEW75ceonJ8GR16O7j86DZfV4Ts1fwT3Jk130_assertion description "[Germline mutations in NKX2-5, GATA4, and CRELD1 are rare in a Mexican sample of Down syndrome patients with endocardial cushion and septal heart defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249428.RAYEArGLeoLwEW75ceonJ8GR16O7j86DZfV4Ts1fwT3Jk130_provenance.
- NP1249428.RAYEArGLeoLwEW75ceonJ8GR16O7j86DZfV4Ts1fwT3Jk130_assertion evidence source_evidence_literature NP1249428.RAYEArGLeoLwEW75ceonJ8GR16O7j86DZfV4Ts1fwT3Jk130_provenance.
- NP1249428.RAYEArGLeoLwEW75ceonJ8GR16O7j86DZfV4Ts1fwT3Jk130_assertion SIO_000772 25524324 NP1249428.RAYEArGLeoLwEW75ceonJ8GR16O7j86DZfV4Ts1fwT3Jk130_provenance.
- NP1249428.RAYEArGLeoLwEW75ceonJ8GR16O7j86DZfV4Ts1fwT3Jk130_assertion wasDerivedFrom befree-2016 NP1249428.RAYEArGLeoLwEW75ceonJ8GR16O7j86DZfV4Ts1fwT3Jk130_provenance.
- NP1249428.RAYEArGLeoLwEW75ceonJ8GR16O7j86DZfV4Ts1fwT3Jk130_assertion wasGeneratedBy ECO_0000203 NP1249428.RAYEArGLeoLwEW75ceonJ8GR16O7j86DZfV4Ts1fwT3Jk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1249428.RAYEArGLeoLwEW75ceonJ8GR16O7j86DZfV4Ts1fwT3Jk130_provenance.