Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP193367.RAWgM8w5hoJkv8dXW52QcTV8GyzYB7HeKTAJE4xVOFe8I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP193367.RAWgM8w5hoJkv8dXW52QcTV8GyzYB7HeKTAJE4xVOFe8I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193367.RAWgM8w5hoJkv8dXW52QcTV8GyzYB7HeKTAJE4xVOFe8I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193367.RAWgM8w5hoJkv8dXW52QcTV8GyzYB7HeKTAJE4xVOFe8I130_provenance.
- NP193367.RAWgM8w5hoJkv8dXW52QcTV8GyzYB7HeKTAJE4xVOFe8I130_assertion description "[Analysis of the three-dimensional structure of the DNA binding runt domain of the RUNX2 protein and its interaction with DNA provide insight into how missense mutations affect RUNX2 function and cause cleidocranial dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193367.RAWgM8w5hoJkv8dXW52QcTV8GyzYB7HeKTAJE4xVOFe8I130_provenance.
- NP193367.RAWgM8w5hoJkv8dXW52QcTV8GyzYB7HeKTAJE4xVOFe8I130_assertion evidence source_evidence_literature NP193367.RAWgM8w5hoJkv8dXW52QcTV8GyzYB7HeKTAJE4xVOFe8I130_provenance.
- NP193367.RAWgM8w5hoJkv8dXW52QcTV8GyzYB7HeKTAJE4xVOFe8I130_assertion SIO_000772 11857736 NP193367.RAWgM8w5hoJkv8dXW52QcTV8GyzYB7HeKTAJE4xVOFe8I130_provenance.
- NP193367.RAWgM8w5hoJkv8dXW52QcTV8GyzYB7HeKTAJE4xVOFe8I130_assertion wasDerivedFrom lhgdn-20090331 NP193367.RAWgM8w5hoJkv8dXW52QcTV8GyzYB7HeKTAJE4xVOFe8I130_provenance.
- NP193367.RAWgM8w5hoJkv8dXW52QcTV8GyzYB7HeKTAJE4xVOFe8I130_assertion wasGeneratedBy ECO_0000203 NP193367.RAWgM8w5hoJkv8dXW52QcTV8GyzYB7HeKTAJE4xVOFe8I130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP193367.RAWgM8w5hoJkv8dXW52QcTV8GyzYB7HeKTAJE4xVOFe8I130_provenance.