Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP867531.RADZFMVi6JBDIWnXPrg6Xz5LZBdeQf6EZMCkZc9YBlYAo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP867531.RADZFMVi6JBDIWnXPrg6Xz5LZBdeQf6EZMCkZc9YBlYAo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867531.RADZFMVi6JBDIWnXPrg6Xz5LZBdeQf6EZMCkZc9YBlYAo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867531.RADZFMVi6JBDIWnXPrg6Xz5LZBdeQf6EZMCkZc9YBlYAo130_provenance.
- NP867531.RADZFMVi6JBDIWnXPrg6Xz5LZBdeQf6EZMCkZc9YBlYAo130_assertion wasGeneratedBy ECO_0000203 NP867531.RADZFMVi6JBDIWnXPrg6Xz5LZBdeQf6EZMCkZc9YBlYAo130_provenance.
- NP867531.RADZFMVi6JBDIWnXPrg6Xz5LZBdeQf6EZMCkZc9YBlYAo130_assertion wasDerivedFrom befree-20140225 NP867531.RADZFMVi6JBDIWnXPrg6Xz5LZBdeQf6EZMCkZc9YBlYAo130_provenance.
- NP867531.RADZFMVi6JBDIWnXPrg6Xz5LZBdeQf6EZMCkZc9YBlYAo130_assertion SIO_000772 15160522 NP867531.RADZFMVi6JBDIWnXPrg6Xz5LZBdeQf6EZMCkZc9YBlYAo130_provenance.
- NP867531.RADZFMVi6JBDIWnXPrg6Xz5LZBdeQf6EZMCkZc9YBlYAo130_assertion evidence source_evidence_literature NP867531.RADZFMVi6JBDIWnXPrg6Xz5LZBdeQf6EZMCkZc9YBlYAo130_provenance.
- NP867531.RADZFMVi6JBDIWnXPrg6Xz5LZBdeQf6EZMCkZc9YBlYAo130_assertion description "[Loss of heterozygosity in the 9p21-p22 region, has been frequently described in a wide range of human malignancies, including familial melanomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867531.RADZFMVi6JBDIWnXPrg6Xz5LZBdeQf6EZMCkZc9YBlYAo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP867531.RADZFMVi6JBDIWnXPrg6Xz5LZBdeQf6EZMCkZc9YBlYAo130_provenance.