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- source_evidence_literature type ECO_0000212 NP187789.RAj5KswtcaYSWYxEBMyZMtJsapHQPZNoDLQIlpLeMv9ug130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP187789.RAj5KswtcaYSWYxEBMyZMtJsapHQPZNoDLQIlpLeMv9ug130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP187789.RAj5KswtcaYSWYxEBMyZMtJsapHQPZNoDLQIlpLeMv9ug130_provenance.
- NP187789.RAj5KswtcaYSWYxEBMyZMtJsapHQPZNoDLQIlpLeMv9ug130_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." NP187789.RAj5KswtcaYSWYxEBMyZMtJsapHQPZNoDLQIlpLeMv9ug130_provenance.
- NP187789.RAj5KswtcaYSWYxEBMyZMtJsapHQPZNoDLQIlpLeMv9ug130_assertion evidence source_evidence_literature NP187789.RAj5KswtcaYSWYxEBMyZMtJsapHQPZNoDLQIlpLeMv9ug130_provenance.
- NP187789.RAj5KswtcaYSWYxEBMyZMtJsapHQPZNoDLQIlpLeMv9ug130_assertion SIO_000772 21039223 NP187789.RAj5KswtcaYSWYxEBMyZMtJsapHQPZNoDLQIlpLeMv9ug130_provenance.
- NP187789.RAj5KswtcaYSWYxEBMyZMtJsapHQPZNoDLQIlpLeMv9ug130_assertion wasDerivedFrom gad-20150221 NP187789.RAj5KswtcaYSWYxEBMyZMtJsapHQPZNoDLQIlpLeMv9ug130_provenance.
- NP187789.RAj5KswtcaYSWYxEBMyZMtJsapHQPZNoDLQIlpLeMv9ug130_assertion wasGeneratedBy ECO_0000203 NP187789.RAj5KswtcaYSWYxEBMyZMtJsapHQPZNoDLQIlpLeMv9ug130_provenance.
- gad-20150221 importedOn "2015-02-21" NP187789.RAj5KswtcaYSWYxEBMyZMtJsapHQPZNoDLQIlpLeMv9ug130_provenance.