Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP51604.RAmr9Q9jLCp7FKGuUJ5p_cmu1t6DrO_gGsrYSg6uvrmlU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP51604.RAmr9Q9jLCp7FKGuUJ5p_cmu1t6DrO_gGsrYSg6uvrmlU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP51604.RAmr9Q9jLCp7FKGuUJ5p_cmu1t6DrO_gGsrYSg6uvrmlU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP51604.RAmr9Q9jLCp7FKGuUJ5p_cmu1t6DrO_gGsrYSg6uvrmlU130_provenance.
- NP51604.RAmr9Q9jLCp7FKGuUJ5p_cmu1t6DrO_gGsrYSg6uvrmlU130_assertion description "[The SLC6A2 haplotype map and 25-marker panel (excluding the monomorphic one) is a comprehensive tool for genetic linkage studies on phenotypes related to NET function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51604.RAmr9Q9jLCp7FKGuUJ5p_cmu1t6DrO_gGsrYSg6uvrmlU130_provenance.
- NP51604.RAmr9Q9jLCp7FKGuUJ5p_cmu1t6DrO_gGsrYSg6uvrmlU130_assertion evidence source_evidence_literature NP51604.RAmr9Q9jLCp7FKGuUJ5p_cmu1t6DrO_gGsrYSg6uvrmlU130_provenance.
- NP51604.RAmr9Q9jLCp7FKGuUJ5p_cmu1t6DrO_gGsrYSg6uvrmlU130_assertion SIO_000772 15362567 NP51604.RAmr9Q9jLCp7FKGuUJ5p_cmu1t6DrO_gGsrYSg6uvrmlU130_provenance.
- NP51604.RAmr9Q9jLCp7FKGuUJ5p_cmu1t6DrO_gGsrYSg6uvrmlU130_assertion wasDerivedFrom gad-20130706 NP51604.RAmr9Q9jLCp7FKGuUJ5p_cmu1t6DrO_gGsrYSg6uvrmlU130_provenance.
- NP51604.RAmr9Q9jLCp7FKGuUJ5p_cmu1t6DrO_gGsrYSg6uvrmlU130_assertion wasGeneratedBy ECO_0000203 NP51604.RAmr9Q9jLCp7FKGuUJ5p_cmu1t6DrO_gGsrYSg6uvrmlU130_provenance.
- gad-20130706 importedOn "2013-07-06" NP51604.RAmr9Q9jLCp7FKGuUJ5p_cmu1t6DrO_gGsrYSg6uvrmlU130_provenance.