Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP738980.RAlsfD61P4YrQtFPD4FX9K-SMfDirCnXJ57IwAWIqe8pg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP738980.RAlsfD61P4YrQtFPD4FX9K-SMfDirCnXJ57IwAWIqe8pg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP738980.RAlsfD61P4YrQtFPD4FX9K-SMfDirCnXJ57IwAWIqe8pg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP738980.RAlsfD61P4YrQtFPD4FX9K-SMfDirCnXJ57IwAWIqe8pg130_provenance.
- NP738980.RAlsfD61P4YrQtFPD4FX9K-SMfDirCnXJ57IwAWIqe8pg130_assertion description "[Among the associated SNPs, the Beh�et's disease-risk allele in rs2061634 leads to substitution of serine to cysteine at amino acid position 995 (S995C) in the KIAA1529 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP738980.RAlsfD61P4YrQtFPD4FX9K-SMfDirCnXJ57IwAWIqe8pg130_provenance.
- NP738980.RAlsfD61P4YrQtFPD4FX9K-SMfDirCnXJ57IwAWIqe8pg130_assertion evidence source_evidence_literature NP738980.RAlsfD61P4YrQtFPD4FX9K-SMfDirCnXJ57IwAWIqe8pg130_provenance.
- NP738980.RAlsfD61P4YrQtFPD4FX9K-SMfDirCnXJ57IwAWIqe8pg130_assertion SIO_000772 19442274 NP738980.RAlsfD61P4YrQtFPD4FX9K-SMfDirCnXJ57IwAWIqe8pg130_provenance.
- NP738980.RAlsfD61P4YrQtFPD4FX9K-SMfDirCnXJ57IwAWIqe8pg130_assertion wasDerivedFrom befree-2016 NP738980.RAlsfD61P4YrQtFPD4FX9K-SMfDirCnXJ57IwAWIqe8pg130_provenance.
- NP738980.RAlsfD61P4YrQtFPD4FX9K-SMfDirCnXJ57IwAWIqe8pg130_assertion wasGeneratedBy ECO_0000203 NP738980.RAlsfD61P4YrQtFPD4FX9K-SMfDirCnXJ57IwAWIqe8pg130_provenance.
- befree-2016 importedOn "2016-02-19" NP738980.RAlsfD61P4YrQtFPD4FX9K-SMfDirCnXJ57IwAWIqe8pg130_provenance.