Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP816428.RA2OH7gWptB7IYNtDsG5nQmuf4W6r42Tb0mn5qvAL72AE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP816428.RA2OH7gWptB7IYNtDsG5nQmuf4W6r42Tb0mn5qvAL72AE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP816428.RA2OH7gWptB7IYNtDsG5nQmuf4W6r42Tb0mn5qvAL72AE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP816428.RA2OH7gWptB7IYNtDsG5nQmuf4W6r42Tb0mn5qvAL72AE130_provenance.
- befree-2016 importedOn "2016-02-19" NP816428.RA2OH7gWptB7IYNtDsG5nQmuf4W6r42Tb0mn5qvAL72AE130_provenance.
- NP816428.RA2OH7gWptB7IYNtDsG5nQmuf4W6r42Tb0mn5qvAL72AE130_assertion wasGeneratedBy ECO_0000203 NP816428.RA2OH7gWptB7IYNtDsG5nQmuf4W6r42Tb0mn5qvAL72AE130_provenance.
- NP816428.RA2OH7gWptB7IYNtDsG5nQmuf4W6r42Tb0mn5qvAL72AE130_assertion wasDerivedFrom befree-2016 NP816428.RA2OH7gWptB7IYNtDsG5nQmuf4W6r42Tb0mn5qvAL72AE130_provenance.
- NP816428.RA2OH7gWptB7IYNtDsG5nQmuf4W6r42Tb0mn5qvAL72AE130_assertion SIO_000772 20522425 NP816428.RA2OH7gWptB7IYNtDsG5nQmuf4W6r42Tb0mn5qvAL72AE130_provenance.
- NP816428.RA2OH7gWptB7IYNtDsG5nQmuf4W6r42Tb0mn5qvAL72AE130_assertion evidence source_evidence_literature NP816428.RA2OH7gWptB7IYNtDsG5nQmuf4W6r42Tb0mn5qvAL72AE130_provenance.
- NP816428.RA2OH7gWptB7IYNtDsG5nQmuf4W6r42Tb0mn5qvAL72AE130_assertion description "[LBR mutation and nuclear envelope defects in a patient affected with Reynolds syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP816428.RA2OH7gWptB7IYNtDsG5nQmuf4W6r42Tb0mn5qvAL72AE130_provenance.