Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP363489.RA-30s9ZD01eWwzNgPXSnzLWGKu1In9iXQcYJPVq5co-A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP363489.RA-30s9ZD01eWwzNgPXSnzLWGKu1In9iXQcYJPVq5co-A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP363489.RA-30s9ZD01eWwzNgPXSnzLWGKu1In9iXQcYJPVq5co-A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP363489.RA-30s9ZD01eWwzNgPXSnzLWGKu1In9iXQcYJPVq5co-A130_provenance.
- NP363489.RA-30s9ZD01eWwzNgPXSnzLWGKu1In9iXQcYJPVq5co-A130_assertion description "[Hemochromatosis is a recessively inherited disorder caused by a point mutation, C282Y of the HFE gene on chromosome 6p21.3 near the human leukocyte antigen (HLA) locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP363489.RA-30s9ZD01eWwzNgPXSnzLWGKu1In9iXQcYJPVq5co-A130_provenance.
- NP363489.RA-30s9ZD01eWwzNgPXSnzLWGKu1In9iXQcYJPVq5co-A130_assertion evidence source_evidence_literature NP363489.RA-30s9ZD01eWwzNgPXSnzLWGKu1In9iXQcYJPVq5co-A130_provenance.
- NP363489.RA-30s9ZD01eWwzNgPXSnzLWGKu1In9iXQcYJPVq5co-A130_assertion SIO_000772 17924859 NP363489.RA-30s9ZD01eWwzNgPXSnzLWGKu1In9iXQcYJPVq5co-A130_provenance.
- NP363489.RA-30s9ZD01eWwzNgPXSnzLWGKu1In9iXQcYJPVq5co-A130_assertion wasDerivedFrom befree-20140225 NP363489.RA-30s9ZD01eWwzNgPXSnzLWGKu1In9iXQcYJPVq5co-A130_provenance.
- NP363489.RA-30s9ZD01eWwzNgPXSnzLWGKu1In9iXQcYJPVq5co-A130_assertion wasGeneratedBy ECO_0000203 NP363489.RA-30s9ZD01eWwzNgPXSnzLWGKu1In9iXQcYJPVq5co-A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP363489.RA-30s9ZD01eWwzNgPXSnzLWGKu1In9iXQcYJPVq5co-A130_provenance.