Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP640012.RAwT6kQQCLNd0aWZc9cE5fGtM1bZz64XtsRvIxRaM6Bcw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP640012.RAwT6kQQCLNd0aWZc9cE5fGtM1bZz64XtsRvIxRaM6Bcw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP640012.RAwT6kQQCLNd0aWZc9cE5fGtM1bZz64XtsRvIxRaM6Bcw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP640012.RAwT6kQQCLNd0aWZc9cE5fGtM1bZz64XtsRvIxRaM6Bcw130_provenance.
- NP640012.RAwT6kQQCLNd0aWZc9cE5fGtM1bZz64XtsRvIxRaM6Bcw130_assertion description "[DRB1*0301 was a common genetic risk factor for familial and sporadic IIM, but contributed less to the genetic risk of familial IIM (etiologic fraction 0.35 versus 0.51 in sporadic IIM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP640012.RAwT6kQQCLNd0aWZc9cE5fGtM1bZz64XtsRvIxRaM6Bcw130_provenance.
- NP640012.RAwT6kQQCLNd0aWZc9cE5fGtM1bZz64XtsRvIxRaM6Bcw130_assertion evidence source_evidence_literature NP640012.RAwT6kQQCLNd0aWZc9cE5fGtM1bZz64XtsRvIxRaM6Bcw130_provenance.
- NP640012.RAwT6kQQCLNd0aWZc9cE5fGtM1bZz64XtsRvIxRaM6Bcw130_assertion SIO_000772 9550481 NP640012.RAwT6kQQCLNd0aWZc9cE5fGtM1bZz64XtsRvIxRaM6Bcw130_provenance.
- NP640012.RAwT6kQQCLNd0aWZc9cE5fGtM1bZz64XtsRvIxRaM6Bcw130_assertion wasDerivedFrom befree-20140225 NP640012.RAwT6kQQCLNd0aWZc9cE5fGtM1bZz64XtsRvIxRaM6Bcw130_provenance.
- NP640012.RAwT6kQQCLNd0aWZc9cE5fGtM1bZz64XtsRvIxRaM6Bcw130_assertion wasGeneratedBy ECO_0000203 NP640012.RAwT6kQQCLNd0aWZc9cE5fGtM1bZz64XtsRvIxRaM6Bcw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP640012.RAwT6kQQCLNd0aWZc9cE5fGtM1bZz64XtsRvIxRaM6Bcw130_provenance.