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- source_evidence_literature type ECO_0000212 NP297233.RAkkj0gd4sD5Mcxf_K508xMDYmNK7y-w76Tdmt978Gif8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP297233.RAkkj0gd4sD5Mcxf_K508xMDYmNK7y-w76Tdmt978Gif8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP297233.RAkkj0gd4sD5Mcxf_K508xMDYmNK7y-w76Tdmt978Gif8130_provenance.
- NP297233.RAkkj0gd4sD5Mcxf_K508xMDYmNK7y-w76Tdmt978Gif8130_assertion description "[Since the dU suppression test is abnormal in transcobalamin II deficiency and in some congenital disorders of vitamin B12 and folate metabolism, it is very useful in the investigation of obscure anaemias in infancy and childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297233.RAkkj0gd4sD5Mcxf_K508xMDYmNK7y-w76Tdmt978Gif8130_provenance.
- NP297233.RAkkj0gd4sD5Mcxf_K508xMDYmNK7y-w76Tdmt978Gif8130_assertion evidence source_evidence_literature NP297233.RAkkj0gd4sD5Mcxf_K508xMDYmNK7y-w76Tdmt978Gif8130_provenance.
- NP297233.RAkkj0gd4sD5Mcxf_K508xMDYmNK7y-w76Tdmt978Gif8130_assertion SIO_000772 3052662 NP297233.RAkkj0gd4sD5Mcxf_K508xMDYmNK7y-w76Tdmt978Gif8130_provenance.
- NP297233.RAkkj0gd4sD5Mcxf_K508xMDYmNK7y-w76Tdmt978Gif8130_assertion wasDerivedFrom befree-20140225 NP297233.RAkkj0gd4sD5Mcxf_K508xMDYmNK7y-w76Tdmt978Gif8130_provenance.
- NP297233.RAkkj0gd4sD5Mcxf_K508xMDYmNK7y-w76Tdmt978Gif8130_assertion wasGeneratedBy ECO_0000203 NP297233.RAkkj0gd4sD5Mcxf_K508xMDYmNK7y-w76Tdmt978Gif8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP297233.RAkkj0gd4sD5Mcxf_K508xMDYmNK7y-w76Tdmt978Gif8130_provenance.