Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP195080.RAWHv_Df_tgqfSyQRxxTJ9wMi8fwCogmW34UrcueHky-I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP195080.RAWHv_Df_tgqfSyQRxxTJ9wMi8fwCogmW34UrcueHky-I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP195080.RAWHv_Df_tgqfSyQRxxTJ9wMi8fwCogmW34UrcueHky-I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP195080.RAWHv_Df_tgqfSyQRxxTJ9wMi8fwCogmW34UrcueHky-I130_provenance.
- NP195080.RAWHv_Df_tgqfSyQRxxTJ9wMi8fwCogmW34UrcueHky-I130_assertion description "[Perforin missense mutations lead to absent perforin detection and impaired cytotoxicity and underly the diversity of hemophagocytic lymphohistiocytosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP195080.RAWHv_Df_tgqfSyQRxxTJ9wMi8fwCogmW34UrcueHky-I130_provenance.
- NP195080.RAWHv_Df_tgqfSyQRxxTJ9wMi8fwCogmW34UrcueHky-I130_assertion evidence source_evidence_literature NP195080.RAWHv_Df_tgqfSyQRxxTJ9wMi8fwCogmW34UrcueHky-I130_provenance.
- NP195080.RAWHv_Df_tgqfSyQRxxTJ9wMi8fwCogmW34UrcueHky-I130_assertion SIO_000772 16374518 NP195080.RAWHv_Df_tgqfSyQRxxTJ9wMi8fwCogmW34UrcueHky-I130_provenance.
- NP195080.RAWHv_Df_tgqfSyQRxxTJ9wMi8fwCogmW34UrcueHky-I130_assertion wasDerivedFrom lhgdn-20090331 NP195080.RAWHv_Df_tgqfSyQRxxTJ9wMi8fwCogmW34UrcueHky-I130_provenance.
- NP195080.RAWHv_Df_tgqfSyQRxxTJ9wMi8fwCogmW34UrcueHky-I130_assertion wasGeneratedBy ECO_0000203 NP195080.RAWHv_Df_tgqfSyQRxxTJ9wMi8fwCogmW34UrcueHky-I130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP195080.RAWHv_Df_tgqfSyQRxxTJ9wMi8fwCogmW34UrcueHky-I130_provenance.