Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP149155.RAHB71TE9fDbbgxczuOirZ902JwAwout3pRLBohICZWG4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP149155.RAHB71TE9fDbbgxczuOirZ902JwAwout3pRLBohICZWG4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP149155.RAHB71TE9fDbbgxczuOirZ902JwAwout3pRLBohICZWG4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP149155.RAHB71TE9fDbbgxczuOirZ902JwAwout3pRLBohICZWG4130_provenance.
- NP149155.RAHB71TE9fDbbgxczuOirZ902JwAwout3pRLBohICZWG4130_assertion description "[mutations in GPD1-L as a pathogenic cause for a small subset of sudden infant death syndrome via a secondary loss-of-function mechanism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149155.RAHB71TE9fDbbgxczuOirZ902JwAwout3pRLBohICZWG4130_provenance.
- NP149155.RAHB71TE9fDbbgxczuOirZ902JwAwout3pRLBohICZWG4130_assertion evidence source_evidence_literature NP149155.RAHB71TE9fDbbgxczuOirZ902JwAwout3pRLBohICZWG4130_provenance.
- NP149155.RAHB71TE9fDbbgxczuOirZ902JwAwout3pRLBohICZWG4130_assertion SIO_000772 17967976 NP149155.RAHB71TE9fDbbgxczuOirZ902JwAwout3pRLBohICZWG4130_provenance.
- NP149155.RAHB71TE9fDbbgxczuOirZ902JwAwout3pRLBohICZWG4130_assertion wasDerivedFrom lhgdn-20090331 NP149155.RAHB71TE9fDbbgxczuOirZ902JwAwout3pRLBohICZWG4130_provenance.
- NP149155.RAHB71TE9fDbbgxczuOirZ902JwAwout3pRLBohICZWG4130_assertion wasGeneratedBy ECO_0000203 NP149155.RAHB71TE9fDbbgxczuOirZ902JwAwout3pRLBohICZWG4130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP149155.RAHB71TE9fDbbgxczuOirZ902JwAwout3pRLBohICZWG4130_provenance.