Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP90983.RAHQDCw8OE-HrhLdTPsE3C2GFxERG_CCDNN2Tjnow6NMs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP90983.RAHQDCw8OE-HrhLdTPsE3C2GFxERG_CCDNN2Tjnow6NMs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP90983.RAHQDCw8OE-HrhLdTPsE3C2GFxERG_CCDNN2Tjnow6NMs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP90983.RAHQDCw8OE-HrhLdTPsE3C2GFxERG_CCDNN2Tjnow6NMs130_provenance.
- NP90983.RAHQDCw8OE-HrhLdTPsE3C2GFxERG_CCDNN2Tjnow6NMs130_assertion description "[C282Y and H63D mutations together with HLA genetic typing have been performed in Spanish hereditary hemochromatosis (n = 98) and PCT (n = 63) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP90983.RAHQDCw8OE-HrhLdTPsE3C2GFxERG_CCDNN2Tjnow6NMs130_provenance.
- NP90983.RAHQDCw8OE-HrhLdTPsE3C2GFxERG_CCDNN2Tjnow6NMs130_assertion evidence source_evidence_literature NP90983.RAHQDCw8OE-HrhLdTPsE3C2GFxERG_CCDNN2Tjnow6NMs130_provenance.
- NP90983.RAHQDCw8OE-HrhLdTPsE3C2GFxERG_CCDNN2Tjnow6NMs130_assertion SIO_000772 15740492 NP90983.RAHQDCw8OE-HrhLdTPsE3C2GFxERG_CCDNN2Tjnow6NMs130_provenance.
- NP90983.RAHQDCw8OE-HrhLdTPsE3C2GFxERG_CCDNN2Tjnow6NMs130_assertion wasDerivedFrom gad-20150221 NP90983.RAHQDCw8OE-HrhLdTPsE3C2GFxERG_CCDNN2Tjnow6NMs130_provenance.
- NP90983.RAHQDCw8OE-HrhLdTPsE3C2GFxERG_CCDNN2Tjnow6NMs130_assertion wasGeneratedBy ECO_0000203 NP90983.RAHQDCw8OE-HrhLdTPsE3C2GFxERG_CCDNN2Tjnow6NMs130_provenance.
- gad-20150221 importedOn "2015-02-21" NP90983.RAHQDCw8OE-HrhLdTPsE3C2GFxERG_CCDNN2Tjnow6NMs130_provenance.