Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP294104.RAFmdHXSxDkNeZGHZr5Khy1AWRdPSNF0R15GhPYGciR6U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294104.RAFmdHXSxDkNeZGHZr5Khy1AWRdPSNF0R15GhPYGciR6U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294104.RAFmdHXSxDkNeZGHZr5Khy1AWRdPSNF0R15GhPYGciR6U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294104.RAFmdHXSxDkNeZGHZr5Khy1AWRdPSNF0R15GhPYGciR6U130_provenance.
- NP294104.RAFmdHXSxDkNeZGHZr5Khy1AWRdPSNF0R15GhPYGciR6U130_assertion description "[Here we have investigated whether variants in NODAL are present in patients with heterotaxy and/or isolated cardiovascular malformations (CVM) thought to be caused by abnormal heart tube looping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294104.RAFmdHXSxDkNeZGHZr5Khy1AWRdPSNF0R15GhPYGciR6U130_provenance.
- NP294104.RAFmdHXSxDkNeZGHZr5Khy1AWRdPSNF0R15GhPYGciR6U130_assertion evidence source_evidence_literature NP294104.RAFmdHXSxDkNeZGHZr5Khy1AWRdPSNF0R15GhPYGciR6U130_provenance.
- NP294104.RAFmdHXSxDkNeZGHZr5Khy1AWRdPSNF0R15GhPYGciR6U130_assertion SIO_000772 19064609 NP294104.RAFmdHXSxDkNeZGHZr5Khy1AWRdPSNF0R15GhPYGciR6U130_provenance.
- NP294104.RAFmdHXSxDkNeZGHZr5Khy1AWRdPSNF0R15GhPYGciR6U130_assertion wasDerivedFrom befree-20140225 NP294104.RAFmdHXSxDkNeZGHZr5Khy1AWRdPSNF0R15GhPYGciR6U130_provenance.
- NP294104.RAFmdHXSxDkNeZGHZr5Khy1AWRdPSNF0R15GhPYGciR6U130_assertion wasGeneratedBy ECO_0000203 NP294104.RAFmdHXSxDkNeZGHZr5Khy1AWRdPSNF0R15GhPYGciR6U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP294104.RAFmdHXSxDkNeZGHZr5Khy1AWRdPSNF0R15GhPYGciR6U130_provenance.