Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP563986.RAxOUJZyigxsOqy2OoLj3rdF5UDgOHT04dZKnzi0E9o1Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP563986.RAxOUJZyigxsOqy2OoLj3rdF5UDgOHT04dZKnzi0E9o1Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP563986.RAxOUJZyigxsOqy2OoLj3rdF5UDgOHT04dZKnzi0E9o1Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP563986.RAxOUJZyigxsOqy2OoLj3rdF5UDgOHT04dZKnzi0E9o1Y130_provenance.
- NP563986.RAxOUJZyigxsOqy2OoLj3rdF5UDgOHT04dZKnzi0E9o1Y130_assertion description "[When independently analyzed, one of the tested polymorphisms in the SLC22A4 gene at 1672 showed significant association with T1D in our Spanish cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP563986.RAxOUJZyigxsOqy2OoLj3rdF5UDgOHT04dZKnzi0E9o1Y130_provenance.
- NP563986.RAxOUJZyigxsOqy2OoLj3rdF5UDgOHT04dZKnzi0E9o1Y130_assertion evidence source_evidence_literature NP563986.RAxOUJZyigxsOqy2OoLj3rdF5UDgOHT04dZKnzi0E9o1Y130_provenance.
- NP563986.RAxOUJZyigxsOqy2OoLj3rdF5UDgOHT04dZKnzi0E9o1Y130_assertion SIO_000772 16796743 NP563986.RAxOUJZyigxsOqy2OoLj3rdF5UDgOHT04dZKnzi0E9o1Y130_provenance.
- NP563986.RAxOUJZyigxsOqy2OoLj3rdF5UDgOHT04dZKnzi0E9o1Y130_assertion wasDerivedFrom befree-20140225 NP563986.RAxOUJZyigxsOqy2OoLj3rdF5UDgOHT04dZKnzi0E9o1Y130_provenance.
- NP563986.RAxOUJZyigxsOqy2OoLj3rdF5UDgOHT04dZKnzi0E9o1Y130_assertion wasGeneratedBy ECO_0000203 NP563986.RAxOUJZyigxsOqy2OoLj3rdF5UDgOHT04dZKnzi0E9o1Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP563986.RAxOUJZyigxsOqy2OoLj3rdF5UDgOHT04dZKnzi0E9o1Y130_provenance.