Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615882.RAUkJg2RQxW4oWTuUgtRyx2UL2COfzY9uhnNkCZVgaL5E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615882.RAUkJg2RQxW4oWTuUgtRyx2UL2COfzY9uhnNkCZVgaL5E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615882.RAUkJg2RQxW4oWTuUgtRyx2UL2COfzY9uhnNkCZVgaL5E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615882.RAUkJg2RQxW4oWTuUgtRyx2UL2COfzY9uhnNkCZVgaL5E130_provenance.
- NP615882.RAUkJg2RQxW4oWTuUgtRyx2UL2COfzY9uhnNkCZVgaL5E130_assertion description "[Although the association with rs973742 warrants further investigations, these results indicate that the genetic variants of CD1 genes do not contribute markedly to the phenotypic variance of X-ALD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615882.RAUkJg2RQxW4oWTuUgtRyx2UL2COfzY9uhnNkCZVgaL5E130_provenance.
- NP615882.RAUkJg2RQxW4oWTuUgtRyx2UL2COfzY9uhnNkCZVgaL5E130_assertion evidence source_evidence_literature NP615882.RAUkJg2RQxW4oWTuUgtRyx2UL2COfzY9uhnNkCZVgaL5E130_provenance.
- NP615882.RAUkJg2RQxW4oWTuUgtRyx2UL2COfzY9uhnNkCZVgaL5E130_assertion SIO_000772 22253809 NP615882.RAUkJg2RQxW4oWTuUgtRyx2UL2COfzY9uhnNkCZVgaL5E130_provenance.
- NP615882.RAUkJg2RQxW4oWTuUgtRyx2UL2COfzY9uhnNkCZVgaL5E130_assertion wasDerivedFrom befree-20140225 NP615882.RAUkJg2RQxW4oWTuUgtRyx2UL2COfzY9uhnNkCZVgaL5E130_provenance.
- NP615882.RAUkJg2RQxW4oWTuUgtRyx2UL2COfzY9uhnNkCZVgaL5E130_assertion wasGeneratedBy ECO_0000203 NP615882.RAUkJg2RQxW4oWTuUgtRyx2UL2COfzY9uhnNkCZVgaL5E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615882.RAUkJg2RQxW4oWTuUgtRyx2UL2COfzY9uhnNkCZVgaL5E130_provenance.