Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP355764.RAQTfu50048OpCrrfmD2X_BADaVqhGpiIxeCPF6QfgVvg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP355764.RAQTfu50048OpCrrfmD2X_BADaVqhGpiIxeCPF6QfgVvg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP355764.RAQTfu50048OpCrrfmD2X_BADaVqhGpiIxeCPF6QfgVvg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP355764.RAQTfu50048OpCrrfmD2X_BADaVqhGpiIxeCPF6QfgVvg130_provenance.
- NP355764.RAQTfu50048OpCrrfmD2X_BADaVqhGpiIxeCPF6QfgVvg130_assertion description "[As SDH mutations are virtually always germline, we conclude that approximately 15% of all pheochromocytomas or paragangliomas are associated with germline SDH mutation and that immunohistochemistry can be used to triage genetic testing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355764.RAQTfu50048OpCrrfmD2X_BADaVqhGpiIxeCPF6QfgVvg130_provenance.
- NP355764.RAQTfu50048OpCrrfmD2X_BADaVqhGpiIxeCPF6QfgVvg130_assertion evidence source_evidence_literature NP355764.RAQTfu50048OpCrrfmD2X_BADaVqhGpiIxeCPF6QfgVvg130_provenance.
- NP355764.RAQTfu50048OpCrrfmD2X_BADaVqhGpiIxeCPF6QfgVvg130_assertion SIO_000772 20236688 NP355764.RAQTfu50048OpCrrfmD2X_BADaVqhGpiIxeCPF6QfgVvg130_provenance.
- NP355764.RAQTfu50048OpCrrfmD2X_BADaVqhGpiIxeCPF6QfgVvg130_assertion wasDerivedFrom befree-20150227 NP355764.RAQTfu50048OpCrrfmD2X_BADaVqhGpiIxeCPF6QfgVvg130_provenance.
- NP355764.RAQTfu50048OpCrrfmD2X_BADaVqhGpiIxeCPF6QfgVvg130_assertion wasGeneratedBy ECO_0000203 NP355764.RAQTfu50048OpCrrfmD2X_BADaVqhGpiIxeCPF6QfgVvg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP355764.RAQTfu50048OpCrrfmD2X_BADaVqhGpiIxeCPF6QfgVvg130_provenance.