Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1090572.RAgi0Wk-3L-OLMgxEgyz5R9T7j_VPMjJO3l8YiPYJWG_E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1090572.RAgi0Wk-3L-OLMgxEgyz5R9T7j_VPMjJO3l8YiPYJWG_E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1090572.RAgi0Wk-3L-OLMgxEgyz5R9T7j_VPMjJO3l8YiPYJWG_E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1090572.RAgi0Wk-3L-OLMgxEgyz5R9T7j_VPMjJO3l8YiPYJWG_E130_provenance.
- NP1090572.RAgi0Wk-3L-OLMgxEgyz5R9T7j_VPMjJO3l8YiPYJWG_E130_assertion description "[Notably, we identified the same FGFR1 mutations in a subset of H3F3A-mutated pediatric glioblastoma with additional alterations in the NF1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1090572.RAgi0Wk-3L-OLMgxEgyz5R9T7j_VPMjJO3l8YiPYJWG_E130_provenance.
- NP1090572.RAgi0Wk-3L-OLMgxEgyz5R9T7j_VPMjJO3l8YiPYJWG_E130_assertion evidence source_evidence_literature NP1090572.RAgi0Wk-3L-OLMgxEgyz5R9T7j_VPMjJO3l8YiPYJWG_E130_provenance.
- NP1090572.RAgi0Wk-3L-OLMgxEgyz5R9T7j_VPMjJO3l8YiPYJWG_E130_assertion SIO_000772 23817572 NP1090572.RAgi0Wk-3L-OLMgxEgyz5R9T7j_VPMjJO3l8YiPYJWG_E130_provenance.
- NP1090572.RAgi0Wk-3L-OLMgxEgyz5R9T7j_VPMjJO3l8YiPYJWG_E130_assertion wasDerivedFrom befree-2016 NP1090572.RAgi0Wk-3L-OLMgxEgyz5R9T7j_VPMjJO3l8YiPYJWG_E130_provenance.
- NP1090572.RAgi0Wk-3L-OLMgxEgyz5R9T7j_VPMjJO3l8YiPYJWG_E130_assertion wasGeneratedBy ECO_0000203 NP1090572.RAgi0Wk-3L-OLMgxEgyz5R9T7j_VPMjJO3l8YiPYJWG_E130_provenance.
- befree-2016 importedOn "2016-02-19" NP1090572.RAgi0Wk-3L-OLMgxEgyz5R9T7j_VPMjJO3l8YiPYJWG_E130_provenance.