Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1381937.RAPMpyyDzVKN7FYrcZDJE9kKay5sV9BIDC7fcVkvHq9Jg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1381937.RAPMpyyDzVKN7FYrcZDJE9kKay5sV9BIDC7fcVkvHq9Jg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1381937.RAPMpyyDzVKN7FYrcZDJE9kKay5sV9BIDC7fcVkvHq9Jg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1381937.RAPMpyyDzVKN7FYrcZDJE9kKay5sV9BIDC7fcVkvHq9Jg130_provenance.
- NP1381937.RAPMpyyDzVKN7FYrcZDJE9kKay5sV9BIDC7fcVkvHq9Jg130_assertion description "[Alleotyping showed loss of heterozygosity (LOH) involving the wild-type alleles in seven tumors in the family including the ependymoma, which is the first MEN1-related case that shows genetic abnormality in chromosome 11q13, suggesting that MEN1 gene might be involved in the tumorigenesis of a subset of ependymomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1381937.RAPMpyyDzVKN7FYrcZDJE9kKay5sV9BIDC7fcVkvHq9Jg130_provenance.
- NP1381937.RAPMpyyDzVKN7FYrcZDJE9kKay5sV9BIDC7fcVkvHq9Jg130_assertion evidence source_evidence_literature NP1381937.RAPMpyyDzVKN7FYrcZDJE9kKay5sV9BIDC7fcVkvHq9Jg130_provenance.
- NP1381937.RAPMpyyDzVKN7FYrcZDJE9kKay5sV9BIDC7fcVkvHq9Jg130_assertion SIO_000772 9329390 NP1381937.RAPMpyyDzVKN7FYrcZDJE9kKay5sV9BIDC7fcVkvHq9Jg130_provenance.
- NP1381937.RAPMpyyDzVKN7FYrcZDJE9kKay5sV9BIDC7fcVkvHq9Jg130_assertion wasDerivedFrom befree-2016 NP1381937.RAPMpyyDzVKN7FYrcZDJE9kKay5sV9BIDC7fcVkvHq9Jg130_provenance.
- NP1381937.RAPMpyyDzVKN7FYrcZDJE9kKay5sV9BIDC7fcVkvHq9Jg130_assertion wasGeneratedBy ECO_0000203 NP1381937.RAPMpyyDzVKN7FYrcZDJE9kKay5sV9BIDC7fcVkvHq9Jg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1381937.RAPMpyyDzVKN7FYrcZDJE9kKay5sV9BIDC7fcVkvHq9Jg130_provenance.