Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615504.RAlgNkq0T_jrr7D7-04S11IyETxLY4dRtkV3eTgBqU2eg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615504.RAlgNkq0T_jrr7D7-04S11IyETxLY4dRtkV3eTgBqU2eg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615504.RAlgNkq0T_jrr7D7-04S11IyETxLY4dRtkV3eTgBqU2eg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615504.RAlgNkq0T_jrr7D7-04S11IyETxLY4dRtkV3eTgBqU2eg130_provenance.
- NP615504.RAlgNkq0T_jrr7D7-04S11IyETxLY4dRtkV3eTgBqU2eg130_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." NP615504.RAlgNkq0T_jrr7D7-04S11IyETxLY4dRtkV3eTgBqU2eg130_provenance.
- NP615504.RAlgNkq0T_jrr7D7-04S11IyETxLY4dRtkV3eTgBqU2eg130_assertion evidence source_evidence_literature NP615504.RAlgNkq0T_jrr7D7-04S11IyETxLY4dRtkV3eTgBqU2eg130_provenance.
- NP615504.RAlgNkq0T_jrr7D7-04S11IyETxLY4dRtkV3eTgBqU2eg130_assertion SIO_000772 9329390 NP615504.RAlgNkq0T_jrr7D7-04S11IyETxLY4dRtkV3eTgBqU2eg130_provenance.
- NP615504.RAlgNkq0T_jrr7D7-04S11IyETxLY4dRtkV3eTgBqU2eg130_assertion wasDerivedFrom befree-20140225 NP615504.RAlgNkq0T_jrr7D7-04S11IyETxLY4dRtkV3eTgBqU2eg130_provenance.
- NP615504.RAlgNkq0T_jrr7D7-04S11IyETxLY4dRtkV3eTgBqU2eg130_assertion wasGeneratedBy ECO_0000203 NP615504.RAlgNkq0T_jrr7D7-04S11IyETxLY4dRtkV3eTgBqU2eg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615504.RAlgNkq0T_jrr7D7-04S11IyETxLY4dRtkV3eTgBqU2eg130_provenance.