Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP173383.RAzjO7BiR99z6up1zfn7XJzKslXui2mSTjGYF1XjN0Czo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP173383.RAzjO7BiR99z6up1zfn7XJzKslXui2mSTjGYF1XjN0Czo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP173383.RAzjO7BiR99z6up1zfn7XJzKslXui2mSTjGYF1XjN0Czo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP173383.RAzjO7BiR99z6up1zfn7XJzKslXui2mSTjGYF1XjN0Czo130_provenance.
- NP173383.RAzjO7BiR99z6up1zfn7XJzKslXui2mSTjGYF1XjN0Czo130_assertion description "[Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173383.RAzjO7BiR99z6up1zfn7XJzKslXui2mSTjGYF1XjN0Czo130_provenance.
- NP173383.RAzjO7BiR99z6up1zfn7XJzKslXui2mSTjGYF1XjN0Czo130_assertion evidence source_evidence_literature NP173383.RAzjO7BiR99z6up1zfn7XJzKslXui2mSTjGYF1XjN0Czo130_provenance.
- NP173383.RAzjO7BiR99z6up1zfn7XJzKslXui2mSTjGYF1XjN0Czo130_assertion SIO_000772 20412296 NP173383.RAzjO7BiR99z6up1zfn7XJzKslXui2mSTjGYF1XjN0Czo130_provenance.
- NP173383.RAzjO7BiR99z6up1zfn7XJzKslXui2mSTjGYF1XjN0Czo130_assertion wasDerivedFrom gad-20150221 NP173383.RAzjO7BiR99z6up1zfn7XJzKslXui2mSTjGYF1XjN0Czo130_provenance.
- NP173383.RAzjO7BiR99z6up1zfn7XJzKslXui2mSTjGYF1XjN0Czo130_assertion wasGeneratedBy ECO_0000203 NP173383.RAzjO7BiR99z6up1zfn7XJzKslXui2mSTjGYF1XjN0Czo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP173383.RAzjO7BiR99z6up1zfn7XJzKslXui2mSTjGYF1XjN0Czo130_provenance.