Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP856828.RA0VG54yHhR3De5otPNaeRl88D3xhWbwkffhToDTcOtkw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP856828.RA0VG54yHhR3De5otPNaeRl88D3xhWbwkffhToDTcOtkw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP856828.RA0VG54yHhR3De5otPNaeRl88D3xhWbwkffhToDTcOtkw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP856828.RA0VG54yHhR3De5otPNaeRl88D3xhWbwkffhToDTcOtkw130_provenance.
- NP856828.RA0VG54yHhR3De5otPNaeRl88D3xhWbwkffhToDTcOtkw130_assertion description "[Genetic defects in human pericentrin (PCNT), encoding the centrosomal protein pericentrin, cause a form of osteodysplastic primordial dwarfism that is sometimes reported to be associated with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856828.RA0VG54yHhR3De5otPNaeRl88D3xhWbwkffhToDTcOtkw130_provenance.
- NP856828.RA0VG54yHhR3De5otPNaeRl88D3xhWbwkffhToDTcOtkw130_assertion evidence source_evidence_literature NP856828.RA0VG54yHhR3De5otPNaeRl88D3xhWbwkffhToDTcOtkw130_provenance.
- NP856828.RA0VG54yHhR3De5otPNaeRl88D3xhWbwkffhToDTcOtkw130_assertion SIO_000772 21270239 NP856828.RA0VG54yHhR3De5otPNaeRl88D3xhWbwkffhToDTcOtkw130_provenance.
- NP856828.RA0VG54yHhR3De5otPNaeRl88D3xhWbwkffhToDTcOtkw130_assertion wasDerivedFrom befree-20140225 NP856828.RA0VG54yHhR3De5otPNaeRl88D3xhWbwkffhToDTcOtkw130_provenance.
- NP856828.RA0VG54yHhR3De5otPNaeRl88D3xhWbwkffhToDTcOtkw130_assertion wasGeneratedBy ECO_0000203 NP856828.RA0VG54yHhR3De5otPNaeRl88D3xhWbwkffhToDTcOtkw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP856828.RA0VG54yHhR3De5otPNaeRl88D3xhWbwkffhToDTcOtkw130_provenance.