Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_provenance.
- NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_assertion description "[The celtic coincidence--the frequency and clinical characterisation of hereditary haemochromatosis in patients with coeliac disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_provenance.
- NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_assertion evidence source_evidence_literature NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_provenance.
- NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_assertion SIO_000772 16615226 NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_provenance.
- NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_assertion wasDerivedFrom gad-20150221 NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_provenance.
- NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_assertion wasGeneratedBy ECO_0000203 NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_provenance.