Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130_provenance.
- NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130_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." NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130_provenance.
- NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130_assertion evidence source_evidence_literature NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130_provenance.
- NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130_assertion SIO_000772 21039223 NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130_provenance.
- NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130_assertion wasDerivedFrom gad-20130706 NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130_provenance.
- NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130_assertion wasGeneratedBy ECO_0000203 NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130_provenance.
- gad-20130706 importedOn "2013-07-06" NP67370.RAW2RbxwXfdMnWt2QFbEn-GK5oZPi4disIAeUVnSyCIng130_provenance.