Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP358016.RArXgk-TnEaW7g0HhQX9fxTnU2gcEesc5IU2IpaeyDUqA130_assertion> ?p ?o ?g. }
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- NP358016.RArXgk-TnEaW7g0HhQX9fxTnU2gcEesc5IU2IpaeyDUqA130_assertion type Assertion NP358016.RArXgk-TnEaW7g0HhQX9fxTnU2gcEesc5IU2IpaeyDUqA130_head.
- NP358016.RArXgk-TnEaW7g0HhQX9fxTnU2gcEesc5IU2IpaeyDUqA130_assertion description "[We report here that a subset of children with medulloblastoma carry germline and somatic mutations in SUFU (encoding the human suppressor of fused) of the SHH pathway, accompanied by loss of heterozygosity of the wildtype allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358016.RArXgk-TnEaW7g0HhQX9fxTnU2gcEesc5IU2IpaeyDUqA130_provenance.
- NP358016.RArXgk-TnEaW7g0HhQX9fxTnU2gcEesc5IU2IpaeyDUqA130_assertion evidence source_evidence_literature NP358016.RArXgk-TnEaW7g0HhQX9fxTnU2gcEesc5IU2IpaeyDUqA130_provenance.
- NP358016.RArXgk-TnEaW7g0HhQX9fxTnU2gcEesc5IU2IpaeyDUqA130_assertion SIO_000772 12068298 NP358016.RArXgk-TnEaW7g0HhQX9fxTnU2gcEesc5IU2IpaeyDUqA130_provenance.
- NP358016.RArXgk-TnEaW7g0HhQX9fxTnU2gcEesc5IU2IpaeyDUqA130_assertion wasDerivedFrom befree-2016 NP358016.RArXgk-TnEaW7g0HhQX9fxTnU2gcEesc5IU2IpaeyDUqA130_provenance.
- NP358016.RArXgk-TnEaW7g0HhQX9fxTnU2gcEesc5IU2IpaeyDUqA130_assertion wasGeneratedBy ECO_0000203 NP358016.RArXgk-TnEaW7g0HhQX9fxTnU2gcEesc5IU2IpaeyDUqA130_provenance.