Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP712809.RA-jglT331hYNd01HzntyCAcNBDZFq4lQXcc4pWL2pJ6A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP712809.RA-jglT331hYNd01HzntyCAcNBDZFq4lQXcc4pWL2pJ6A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP712809.RA-jglT331hYNd01HzntyCAcNBDZFq4lQXcc4pWL2pJ6A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP712809.RA-jglT331hYNd01HzntyCAcNBDZFq4lQXcc4pWL2pJ6A130_provenance.
- NP712809.RA-jglT331hYNd01HzntyCAcNBDZFq4lQXcc4pWL2pJ6A130_assertion description "[However, overexpressed p48 peptides containing the mutations found in three Ddb(-) XPE strains are inactive, and wild type p48 restores DDB activity to extracts from a fourth XPE Ddb(-) strain, GM01389, in which compound heterozygous mutations in DDB2 (p48) lead to a L350P change from one allele and a Asn-349 deletion from the other.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP712809.RA-jglT331hYNd01HzntyCAcNBDZFq4lQXcc4pWL2pJ6A130_provenance.
- NP712809.RA-jglT331hYNd01HzntyCAcNBDZFq4lQXcc4pWL2pJ6A130_assertion evidence source_evidence_literature NP712809.RA-jglT331hYNd01HzntyCAcNBDZFq4lQXcc4pWL2pJ6A130_provenance.
- NP712809.RA-jglT331hYNd01HzntyCAcNBDZFq4lQXcc4pWL2pJ6A130_assertion SIO_000772 10777490 NP712809.RA-jglT331hYNd01HzntyCAcNBDZFq4lQXcc4pWL2pJ6A130_provenance.
- NP712809.RA-jglT331hYNd01HzntyCAcNBDZFq4lQXcc4pWL2pJ6A130_assertion wasDerivedFrom befree-20140225 NP712809.RA-jglT331hYNd01HzntyCAcNBDZFq4lQXcc4pWL2pJ6A130_provenance.
- NP712809.RA-jglT331hYNd01HzntyCAcNBDZFq4lQXcc4pWL2pJ6A130_assertion wasGeneratedBy ECO_0000203 NP712809.RA-jglT331hYNd01HzntyCAcNBDZFq4lQXcc4pWL2pJ6A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP712809.RA-jglT331hYNd01HzntyCAcNBDZFq4lQXcc4pWL2pJ6A130_provenance.