Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP246363.RAEAi5Ck7pUSdsaofVQ1Ah0eW1ST6CBCgxQIQfRqsAGuc130_assertion> ?p ?o ?g. }
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- NP246363.RAEAi5Ck7pUSdsaofVQ1Ah0eW1ST6CBCgxQIQfRqsAGuc130_assertion type Assertion NP246363.RAEAi5Ck7pUSdsaofVQ1Ah0eW1ST6CBCgxQIQfRqsAGuc130_head.
- NP246363.RAEAi5Ck7pUSdsaofVQ1Ah0eW1ST6CBCgxQIQfRqsAGuc130_assertion description "[There was a significantly higher frequency of coinheritance of the hereditary hemochromatosis (HH) HFE mutant allele C282Y in 18 unrelated XLSA hemizygotes than found in the normal population, indicating a role for coinheritance of HFE alleles in the expression of this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP246363.RAEAi5Ck7pUSdsaofVQ1Ah0eW1ST6CBCgxQIQfRqsAGuc130_provenance.
- NP246363.RAEAi5Ck7pUSdsaofVQ1Ah0eW1ST6CBCgxQIQfRqsAGuc130_assertion evidence source_evidence_literature NP246363.RAEAi5Ck7pUSdsaofVQ1Ah0eW1ST6CBCgxQIQfRqsAGuc130_provenance.
- NP246363.RAEAi5Ck7pUSdsaofVQ1Ah0eW1ST6CBCgxQIQfRqsAGuc130_assertion SIO_000772 10029606 NP246363.RAEAi5Ck7pUSdsaofVQ1Ah0eW1ST6CBCgxQIQfRqsAGuc130_provenance.
- NP246363.RAEAi5Ck7pUSdsaofVQ1Ah0eW1ST6CBCgxQIQfRqsAGuc130_assertion wasDerivedFrom befree-2016 NP246363.RAEAi5Ck7pUSdsaofVQ1Ah0eW1ST6CBCgxQIQfRqsAGuc130_provenance.
- NP246363.RAEAi5Ck7pUSdsaofVQ1Ah0eW1ST6CBCgxQIQfRqsAGuc130_assertion wasGeneratedBy ECO_0000203 NP246363.RAEAi5Ck7pUSdsaofVQ1Ah0eW1ST6CBCgxQIQfRqsAGuc130_provenance.