Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP52486.RAw5DDM5AhPjeRlRvVElhRrb6xQlz2aAICMx3zWgnDl7Y130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP52486.RAw5DDM5AhPjeRlRvVElhRrb6xQlz2aAICMx3zWgnDl7Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52486.RAw5DDM5AhPjeRlRvVElhRrb6xQlz2aAICMx3zWgnDl7Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52486.RAw5DDM5AhPjeRlRvVElhRrb6xQlz2aAICMx3zWgnDl7Y130_provenance.
- NP52486.RAw5DDM5AhPjeRlRvVElhRrb6xQlz2aAICMx3zWgnDl7Y130_assertion description "[Fourteen NS patients, half of them with PTPN11 mutations in heterozygous state, were studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52486.RAw5DDM5AhPjeRlRvVElhRrb6xQlz2aAICMx3zWgnDl7Y130_provenance.
- NP52486.RAw5DDM5AhPjeRlRvVElhRrb6xQlz2aAICMx3zWgnDl7Y130_assertion evidence source_evidence_literature NP52486.RAw5DDM5AhPjeRlRvVElhRrb6xQlz2aAICMx3zWgnDl7Y130_provenance.
- NP52486.RAw5DDM5AhPjeRlRvVElhRrb6xQlz2aAICMx3zWgnDl7Y130_assertion SIO_000772 15956085 NP52486.RAw5DDM5AhPjeRlRvVElhRrb6xQlz2aAICMx3zWgnDl7Y130_provenance.
- NP52486.RAw5DDM5AhPjeRlRvVElhRrb6xQlz2aAICMx3zWgnDl7Y130_assertion wasDerivedFrom gad-20130706 NP52486.RAw5DDM5AhPjeRlRvVElhRrb6xQlz2aAICMx3zWgnDl7Y130_provenance.
- NP52486.RAw5DDM5AhPjeRlRvVElhRrb6xQlz2aAICMx3zWgnDl7Y130_assertion wasGeneratedBy ECO_0000203 NP52486.RAw5DDM5AhPjeRlRvVElhRrb6xQlz2aAICMx3zWgnDl7Y130_provenance.
- gad-20130706 importedOn "2013-07-06" NP52486.RAw5DDM5AhPjeRlRvVElhRrb6xQlz2aAICMx3zWgnDl7Y130_provenance.