Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_provenance.
- NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_assertion description "[To study the prevalence of homozygotic H63D mutation in patients with phenotypic hemochromatosis (PH) and to compare the results with those of the general population and with patients with porphyria cutanea tarda (PCT) in the Basque Country, Spain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_provenance.
- NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_assertion evidence source_evidence_literature NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_provenance.
- NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_assertion SIO_000772 20594259 NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_provenance.
- NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_assertion wasDerivedFrom gad-20150221 NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_provenance.
- NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_assertion wasGeneratedBy ECO_0000203 NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP180299.RAXSI4nkiLVZrvi1fvB36-tHW7Jd1ES3B_F8rirYkFtAo130_provenance.