Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP439882.RAQFRmvxN3dkTgTvE7pmMP1Jia7a5CHlBK_3PKThxhly8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP439882.RAQFRmvxN3dkTgTvE7pmMP1Jia7a5CHlBK_3PKThxhly8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP439882.RAQFRmvxN3dkTgTvE7pmMP1Jia7a5CHlBK_3PKThxhly8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP439882.RAQFRmvxN3dkTgTvE7pmMP1Jia7a5CHlBK_3PKThxhly8130_provenance.
- NP439882.RAQFRmvxN3dkTgTvE7pmMP1Jia7a5CHlBK_3PKThxhly8130_assertion wasGeneratedBy ECO_0000203 NP439882.RAQFRmvxN3dkTgTvE7pmMP1Jia7a5CHlBK_3PKThxhly8130_provenance.
- NP439882.RAQFRmvxN3dkTgTvE7pmMP1Jia7a5CHlBK_3PKThxhly8130_assertion wasDerivedFrom befree-20140225 NP439882.RAQFRmvxN3dkTgTvE7pmMP1Jia7a5CHlBK_3PKThxhly8130_provenance.
- NP439882.RAQFRmvxN3dkTgTvE7pmMP1Jia7a5CHlBK_3PKThxhly8130_assertion SIO_000772 18654888 NP439882.RAQFRmvxN3dkTgTvE7pmMP1Jia7a5CHlBK_3PKThxhly8130_provenance.
- NP439882.RAQFRmvxN3dkTgTvE7pmMP1Jia7a5CHlBK_3PKThxhly8130_assertion evidence source_evidence_literature NP439882.RAQFRmvxN3dkTgTvE7pmMP1Jia7a5CHlBK_3PKThxhly8130_provenance.
- NP439882.RAQFRmvxN3dkTgTvE7pmMP1Jia7a5CHlBK_3PKThxhly8130_assertion description "[In all four cases (two unrelated children and two siblings), DNA analysis identified common alpha(+)-thalassemia (alpha(+)-thal) mutations in trans to the in frame 3 bp deletion (-CCC) on the alpha1-globin gene between codons 36 and 37, which has previously been reported as Hb Heraklion in a single Greek case.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP439882.RAQFRmvxN3dkTgTvE7pmMP1Jia7a5CHlBK_3PKThxhly8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP439882.RAQFRmvxN3dkTgTvE7pmMP1Jia7a5CHlBK_3PKThxhly8130_provenance.