Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP734588.RAawN4fo8qSeLloZlgmFk2q9P-wGIlZAJb29-nfSb_vSI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP734588.RAawN4fo8qSeLloZlgmFk2q9P-wGIlZAJb29-nfSb_vSI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734588.RAawN4fo8qSeLloZlgmFk2q9P-wGIlZAJb29-nfSb_vSI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734588.RAawN4fo8qSeLloZlgmFk2q9P-wGIlZAJb29-nfSb_vSI130_provenance.
- NP734588.RAawN4fo8qSeLloZlgmFk2q9P-wGIlZAJb29-nfSb_vSI130_assertion description "[All samples were analysed by DNA array analysis (HEA Beadchip(TM), Bioarray Solutions) to determine polymorphisms associated with antigen expression for 11 blood group systems (Rh, Kell, Kidd, Duffy, MNS, Dombrock, Lutheran, Landsteiner-Wiener, Diego, Colton, Scianna); and one mutation associated with haemoglobinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734588.RAawN4fo8qSeLloZlgmFk2q9P-wGIlZAJb29-nfSb_vSI130_provenance.
- NP734588.RAawN4fo8qSeLloZlgmFk2q9P-wGIlZAJb29-nfSb_vSI130_assertion evidence source_evidence_literature NP734588.RAawN4fo8qSeLloZlgmFk2q9P-wGIlZAJb29-nfSb_vSI130_provenance.
- NP734588.RAawN4fo8qSeLloZlgmFk2q9P-wGIlZAJb29-nfSb_vSI130_assertion SIO_000772 19392786 NP734588.RAawN4fo8qSeLloZlgmFk2q9P-wGIlZAJb29-nfSb_vSI130_provenance.
- NP734588.RAawN4fo8qSeLloZlgmFk2q9P-wGIlZAJb29-nfSb_vSI130_assertion wasDerivedFrom befree-2016 NP734588.RAawN4fo8qSeLloZlgmFk2q9P-wGIlZAJb29-nfSb_vSI130_provenance.
- NP734588.RAawN4fo8qSeLloZlgmFk2q9P-wGIlZAJb29-nfSb_vSI130_assertion wasGeneratedBy ECO_0000203 NP734588.RAawN4fo8qSeLloZlgmFk2q9P-wGIlZAJb29-nfSb_vSI130_provenance.
- befree-2016 importedOn "2016-02-19" NP734588.RAawN4fo8qSeLloZlgmFk2q9P-wGIlZAJb29-nfSb_vSI130_provenance.