Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_provenance.
- NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_assertion description "[These data matched the clinical observations on patients with SCN5A loss-of-function mutations with either severe or mild conduction defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_provenance.
- NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_assertion evidence source_evidence_literature NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_provenance.
- NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_assertion SIO_000772 20174578 NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_provenance.
- NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_assertion wasDerivedFrom befree-20140225 NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_provenance.
- NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_assertion wasGeneratedBy ECO_0000203 NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_provenance.
- befree-20140225 importedOn "2014-02-25" NP402131.RAdoPIWheVm5LpvUqtE7rkcqXCY49qvQp8O2BsJJO11Ek130_provenance.