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- source_evidence_literature type ECO_0000212 NP255482.RA6b1YtVfbqRuxBKRTBNrslOFNsYANI4B_Pp2_87XsuXM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP255482.RA6b1YtVfbqRuxBKRTBNrslOFNsYANI4B_Pp2_87XsuXM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP255482.RA6b1YtVfbqRuxBKRTBNrslOFNsYANI4B_Pp2_87XsuXM130_provenance.
- NP255482.RA6b1YtVfbqRuxBKRTBNrslOFNsYANI4B_Pp2_87XsuXM130_assertion description "[Although medulloblastoma is a component of Turcot syndrome with demonstrated APC mutations, APC gene deletions appear to be absent or very uncommon in patients with sporadic and NBCCS-associated medulloblastomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP255482.RA6b1YtVfbqRuxBKRTBNrslOFNsYANI4B_Pp2_87XsuXM130_provenance.
- NP255482.RA6b1YtVfbqRuxBKRTBNrslOFNsYANI4B_Pp2_87XsuXM130_assertion evidence source_evidence_literature NP255482.RA6b1YtVfbqRuxBKRTBNrslOFNsYANI4B_Pp2_87XsuXM130_provenance.
- NP255482.RA6b1YtVfbqRuxBKRTBNrslOFNsYANI4B_Pp2_87XsuXM130_assertion SIO_000772 10375116 NP255482.RA6b1YtVfbqRuxBKRTBNrslOFNsYANI4B_Pp2_87XsuXM130_provenance.
- NP255482.RA6b1YtVfbqRuxBKRTBNrslOFNsYANI4B_Pp2_87XsuXM130_assertion wasDerivedFrom befree-2016 NP255482.RA6b1YtVfbqRuxBKRTBNrslOFNsYANI4B_Pp2_87XsuXM130_provenance.
- NP255482.RA6b1YtVfbqRuxBKRTBNrslOFNsYANI4B_Pp2_87XsuXM130_assertion wasGeneratedBy ECO_0000203 NP255482.RA6b1YtVfbqRuxBKRTBNrslOFNsYANI4B_Pp2_87XsuXM130_provenance.
- befree-2016 importedOn "2016-02-19" NP255482.RA6b1YtVfbqRuxBKRTBNrslOFNsYANI4B_Pp2_87XsuXM130_provenance.