Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP443507.RARU8PF-lI8vOEjOkjPd6mXJQJSEILVA6O24_uL5izFwY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP443507.RARU8PF-lI8vOEjOkjPd6mXJQJSEILVA6O24_uL5izFwY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP443507.RARU8PF-lI8vOEjOkjPd6mXJQJSEILVA6O24_uL5izFwY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP443507.RARU8PF-lI8vOEjOkjPd6mXJQJSEILVA6O24_uL5izFwY130_provenance.
- NP443507.RARU8PF-lI8vOEjOkjPd6mXJQJSEILVA6O24_uL5izFwY130_assertion description "[Since compound heterozygotes for ?-thal and a ?-globin gene mutation may have low mean cell volume (MCV) and normal Hb A(2) levels, and therefore be overlooked as ?-thal heterozygotes, a detailed molecular analysis for both ?- and ?-thal is necessary, especially when one partner has been identified to have ?-thal trait.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP443507.RARU8PF-lI8vOEjOkjPd6mXJQJSEILVA6O24_uL5izFwY130_provenance.
- NP443507.RARU8PF-lI8vOEjOkjPd6mXJQJSEILVA6O24_uL5izFwY130_assertion evidence source_evidence_literature NP443507.RARU8PF-lI8vOEjOkjPd6mXJQJSEILVA6O24_uL5izFwY130_provenance.
- NP443507.RARU8PF-lI8vOEjOkjPd6mXJQJSEILVA6O24_uL5izFwY130_assertion SIO_000772 23215833 NP443507.RARU8PF-lI8vOEjOkjPd6mXJQJSEILVA6O24_uL5izFwY130_provenance.
- NP443507.RARU8PF-lI8vOEjOkjPd6mXJQJSEILVA6O24_uL5izFwY130_assertion wasDerivedFrom befree-20150227 NP443507.RARU8PF-lI8vOEjOkjPd6mXJQJSEILVA6O24_uL5izFwY130_provenance.
- NP443507.RARU8PF-lI8vOEjOkjPd6mXJQJSEILVA6O24_uL5izFwY130_assertion wasGeneratedBy ECO_0000203 NP443507.RARU8PF-lI8vOEjOkjPd6mXJQJSEILVA6O24_uL5izFwY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP443507.RARU8PF-lI8vOEjOkjPd6mXJQJSEILVA6O24_uL5izFwY130_provenance.