Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP248547.RALh40FiSBtW6R380Qc0dWAvC3FzTGYmHC27hYpsQzxQY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP248547.RALh40FiSBtW6R380Qc0dWAvC3FzTGYmHC27hYpsQzxQY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP248547.RALh40FiSBtW6R380Qc0dWAvC3FzTGYmHC27hYpsQzxQY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP248547.RALh40FiSBtW6R380Qc0dWAvC3FzTGYmHC27hYpsQzxQY130_provenance.
- NP248547.RALh40FiSBtW6R380Qc0dWAvC3FzTGYmHC27hYpsQzxQY130_assertion description "[These data suggest that the ALD patient defect involves the Fas signaling pathway downstream from the sphingomyelinase and that Fas gene mutations and double-negative T-cell expansion are not the only signs of a defective Fas system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP248547.RALh40FiSBtW6R380Qc0dWAvC3FzTGYmHC27hYpsQzxQY130_provenance.
- NP248547.RALh40FiSBtW6R380Qc0dWAvC3FzTGYmHC27hYpsQzxQY130_assertion evidence source_evidence_literature NP248547.RALh40FiSBtW6R380Qc0dWAvC3FzTGYmHC27hYpsQzxQY130_provenance.
- NP248547.RALh40FiSBtW6R380Qc0dWAvC3FzTGYmHC27hYpsQzxQY130_assertion SIO_000772 9108407 NP248547.RALh40FiSBtW6R380Qc0dWAvC3FzTGYmHC27hYpsQzxQY130_provenance.
- NP248547.RALh40FiSBtW6R380Qc0dWAvC3FzTGYmHC27hYpsQzxQY130_assertion wasDerivedFrom befree-20150227 NP248547.RALh40FiSBtW6R380Qc0dWAvC3FzTGYmHC27hYpsQzxQY130_provenance.
- NP248547.RALh40FiSBtW6R380Qc0dWAvC3FzTGYmHC27hYpsQzxQY130_assertion wasGeneratedBy ECO_0000203 NP248547.RALh40FiSBtW6R380Qc0dWAvC3FzTGYmHC27hYpsQzxQY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP248547.RALh40FiSBtW6R380Qc0dWAvC3FzTGYmHC27hYpsQzxQY130_provenance.