Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_provenance.
- NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_assertion description "[Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive disorder characterized by juvenile megaloblastic anaemia, as well as neurological symptoms that may be the only manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_provenance.
- NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_assertion evidence source_evidence_literature NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_provenance.
- NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_assertion SIO_000772 10080186 NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_provenance.
- NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_assertion wasDerivedFrom befree-20140225 NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_provenance.
- NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_assertion wasGeneratedBy ECO_0000203 NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_provenance.
- befree-20140225 importedOn "2014-02-25" NP373465.RAlMg9jCNhIR5iTnKunicNdr7WgiJoS0rflmLZHwXeUns130_provenance.