Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_provenance.
- NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_assertion description "[HJV p.A310G polymorphism and two intronic variants were found, but none of these alterations were associated with digenic inheritance with the HFE gene. Our data indicate that HJV and HAMP functional mutations are not frequent in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_provenance.
- NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_assertion evidence source_evidence_literature NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_provenance.
- NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_assertion SIO_000772 21039223 NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_provenance.
- NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_assertion wasDerivedFrom gad-20130706 NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_provenance.
- NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_assertion wasGeneratedBy ECO_0000203 NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_provenance.
- gad-20130706 importedOn "2013-07-06" NP79061.RAkyGKzaa8cwh6Y51PbMQmzoC6n17hJ8hLDUaNp5_SS9I130_provenance.