Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP789151.RAoBMiZywhYPjGJe7_D5hDOp0niBhuGI2Caw-roO3e2cI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP789151.RAoBMiZywhYPjGJe7_D5hDOp0niBhuGI2Caw-roO3e2cI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP789151.RAoBMiZywhYPjGJe7_D5hDOp0niBhuGI2Caw-roO3e2cI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP789151.RAoBMiZywhYPjGJe7_D5hDOp0niBhuGI2Caw-roO3e2cI130_provenance.
- NP789151.RAoBMiZywhYPjGJe7_D5hDOp0niBhuGI2Caw-roO3e2cI130_assertion description "[Mutations of the UROD and hemochromatosis (HFE) genes are genetic factors in some PCT patients which can be mimicked in mice heterozygous for the Hfe and Urod null genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789151.RAoBMiZywhYPjGJe7_D5hDOp0niBhuGI2Caw-roO3e2cI130_provenance.
- NP789151.RAoBMiZywhYPjGJe7_D5hDOp0niBhuGI2Caw-roO3e2cI130_assertion evidence source_evidence_literature NP789151.RAoBMiZywhYPjGJe7_D5hDOp0niBhuGI2Caw-roO3e2cI130_provenance.
- NP789151.RAoBMiZywhYPjGJe7_D5hDOp0niBhuGI2Caw-roO3e2cI130_assertion SIO_000772 20099833 NP789151.RAoBMiZywhYPjGJe7_D5hDOp0niBhuGI2Caw-roO3e2cI130_provenance.
- NP789151.RAoBMiZywhYPjGJe7_D5hDOp0niBhuGI2Caw-roO3e2cI130_assertion wasDerivedFrom befree-2016 NP789151.RAoBMiZywhYPjGJe7_D5hDOp0niBhuGI2Caw-roO3e2cI130_provenance.
- NP789151.RAoBMiZywhYPjGJe7_D5hDOp0niBhuGI2Caw-roO3e2cI130_assertion wasGeneratedBy ECO_0000203 NP789151.RAoBMiZywhYPjGJe7_D5hDOp0niBhuGI2Caw-roO3e2cI130_provenance.
- befree-2016 importedOn "2016-02-19" NP789151.RAoBMiZywhYPjGJe7_D5hDOp0niBhuGI2Caw-roO3e2cI130_provenance.