Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP753316.RAd96YZjVQ3u9bn1WWACKAPO0QxjF8YW7p0ZlQq9r-41Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP753316.RAd96YZjVQ3u9bn1WWACKAPO0QxjF8YW7p0ZlQq9r-41Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP753316.RAd96YZjVQ3u9bn1WWACKAPO0QxjF8YW7p0ZlQq9r-41Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP753316.RAd96YZjVQ3u9bn1WWACKAPO0QxjF8YW7p0ZlQq9r-41Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP753316.RAd96YZjVQ3u9bn1WWACKAPO0QxjF8YW7p0ZlQq9r-41Q130_provenance.
- NP753316.RAd96YZjVQ3u9bn1WWACKAPO0QxjF8YW7p0ZlQq9r-41Q130_assertion wasGeneratedBy ECO_0000203 NP753316.RAd96YZjVQ3u9bn1WWACKAPO0QxjF8YW7p0ZlQq9r-41Q130_provenance.
- NP753316.RAd96YZjVQ3u9bn1WWACKAPO0QxjF8YW7p0ZlQq9r-41Q130_assertion wasDerivedFrom befree-2016 NP753316.RAd96YZjVQ3u9bn1WWACKAPO0QxjF8YW7p0ZlQq9r-41Q130_provenance.
- NP753316.RAd96YZjVQ3u9bn1WWACKAPO0QxjF8YW7p0ZlQq9r-41Q130_assertion SIO_000772 19629396 NP753316.RAd96YZjVQ3u9bn1WWACKAPO0QxjF8YW7p0ZlQq9r-41Q130_provenance.
- NP753316.RAd96YZjVQ3u9bn1WWACKAPO0QxjF8YW7p0ZlQq9r-41Q130_assertion evidence source_evidence_literature NP753316.RAd96YZjVQ3u9bn1WWACKAPO0QxjF8YW7p0ZlQq9r-41Q130_provenance.
- NP753316.RAd96YZjVQ3u9bn1WWACKAPO0QxjF8YW7p0ZlQq9r-41Q130_assertion description "[Because of the low frequency of the mutations identified in the studied group, we were unable to determine the exact role of NBN in the development of astrocytoma in children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP753316.RAd96YZjVQ3u9bn1WWACKAPO0QxjF8YW7p0ZlQq9r-41Q130_provenance.