Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP967947.RAMZfd1SnczTU2OdofRlVtQURV0HJs8f4jhjMvf6S9_-E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP967947.RAMZfd1SnczTU2OdofRlVtQURV0HJs8f4jhjMvf6S9_-E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP967947.RAMZfd1SnczTU2OdofRlVtQURV0HJs8f4jhjMvf6S9_-E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP967947.RAMZfd1SnczTU2OdofRlVtQURV0HJs8f4jhjMvf6S9_-E130_provenance.
- NP967947.RAMZfd1SnczTU2OdofRlVtQURV0HJs8f4jhjMvf6S9_-E130_assertion description "[In Caucasian families from the United States of America and United Kingdom, susceptibility to generalized vitiligo and associated autoimmune diseases is genetically associated with variants of NALP1, encoding NACHT leucine-rich repeat protein 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP967947.RAMZfd1SnczTU2OdofRlVtQURV0HJs8f4jhjMvf6S9_-E130_provenance.
- NP967947.RAMZfd1SnczTU2OdofRlVtQURV0HJs8f4jhjMvf6S9_-E130_assertion evidence source_evidence_literature NP967947.RAMZfd1SnczTU2OdofRlVtQURV0HJs8f4jhjMvf6S9_-E130_provenance.
- NP967947.RAMZfd1SnczTU2OdofRlVtQURV0HJs8f4jhjMvf6S9_-E130_assertion SIO_000772 17637824 NP967947.RAMZfd1SnczTU2OdofRlVtQURV0HJs8f4jhjMvf6S9_-E130_provenance.
- NP967947.RAMZfd1SnczTU2OdofRlVtQURV0HJs8f4jhjMvf6S9_-E130_assertion wasDerivedFrom befree-20150227 NP967947.RAMZfd1SnczTU2OdofRlVtQURV0HJs8f4jhjMvf6S9_-E130_provenance.
- NP967947.RAMZfd1SnczTU2OdofRlVtQURV0HJs8f4jhjMvf6S9_-E130_assertion wasGeneratedBy ECO_0000203 NP967947.RAMZfd1SnczTU2OdofRlVtQURV0HJs8f4jhjMvf6S9_-E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP967947.RAMZfd1SnczTU2OdofRlVtQURV0HJs8f4jhjMvf6S9_-E130_provenance.