Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP434732.RAglk5tVBFnzr-unSqNo7795xmW0bP7MjuKu_tx7hjvIg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434732.RAglk5tVBFnzr-unSqNo7795xmW0bP7MjuKu_tx7hjvIg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434732.RAglk5tVBFnzr-unSqNo7795xmW0bP7MjuKu_tx7hjvIg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434732.RAglk5tVBFnzr-unSqNo7795xmW0bP7MjuKu_tx7hjvIg130_provenance.
- NP434732.RAglk5tVBFnzr-unSqNo7795xmW0bP7MjuKu_tx7hjvIg130_assertion wasGeneratedBy ECO_0000203 NP434732.RAglk5tVBFnzr-unSqNo7795xmW0bP7MjuKu_tx7hjvIg130_provenance.
- NP434732.RAglk5tVBFnzr-unSqNo7795xmW0bP7MjuKu_tx7hjvIg130_assertion wasDerivedFrom befree-20140225 NP434732.RAglk5tVBFnzr-unSqNo7795xmW0bP7MjuKu_tx7hjvIg130_provenance.
- NP434732.RAglk5tVBFnzr-unSqNo7795xmW0bP7MjuKu_tx7hjvIg130_assertion SIO_000772 19500772 NP434732.RAglk5tVBFnzr-unSqNo7795xmW0bP7MjuKu_tx7hjvIg130_provenance.
- NP434732.RAglk5tVBFnzr-unSqNo7795xmW0bP7MjuKu_tx7hjvIg130_assertion evidence source_evidence_literature NP434732.RAglk5tVBFnzr-unSqNo7795xmW0bP7MjuKu_tx7hjvIg130_provenance.
- NP434732.RAglk5tVBFnzr-unSqNo7795xmW0bP7MjuKu_tx7hjvIg130_assertion description "[Subsequently, we have identified four different heterozygous mutations (frameshift, nonsense, and no-stop) in the candidate FOXF1 gene in unrelated patients with sporadic ACD/MPV and MCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434732.RAglk5tVBFnzr-unSqNo7795xmW0bP7MjuKu_tx7hjvIg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP434732.RAglk5tVBFnzr-unSqNo7795xmW0bP7MjuKu_tx7hjvIg130_provenance.