Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130_provenance.
- NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130_assertion description "[Our results suggest that the G908R mutation of the CARD15/NOD2 gene, as well as the T allele and TT genotype of the CD14 promoter are associated with increased susceptibility for developing sarcoidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130_provenance.
- NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130_assertion evidence source_evidence_literature NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130_provenance.
- NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130_assertion SIO_000772 16933467 NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130_provenance.
- NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130_assertion wasDerivedFrom gad-20130706 NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130_provenance.
- NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130_assertion wasGeneratedBy ECO_0000203 NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130_provenance.
- gad-20130706 importedOn "2013-07-06" NP65992.RASfLzzHVVqfaMFuGVtNUeXUd-ENHmReGOnI8o2mBzaSQ130_provenance.