Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP208296.RACbnHAK4PXXurVJYIXK6Va5qrZLLd7iyd3vLmSTSqweQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP208296.RACbnHAK4PXXurVJYIXK6Va5qrZLLd7iyd3vLmSTSqweQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP208296.RACbnHAK4PXXurVJYIXK6Va5qrZLLd7iyd3vLmSTSqweQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP208296.RACbnHAK4PXXurVJYIXK6Va5qrZLLd7iyd3vLmSTSqweQ130_provenance.
- NP208296.RACbnHAK4PXXurVJYIXK6Va5qrZLLd7iyd3vLmSTSqweQ130_assertion description "[This paper will review the genetic and molecular basis of several important bone marrow failure syndromes in children, Fanconi anemia, Shwachman-Diamond syndrome, Diamond-Blackfan anemia, congenital amegakaryocytic thrombocytopenia, dyskeratosis congenita, and severe congenital neutropenia, and the recent discoveries that have enhanced our understanding of the pathogenesis of these diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208296.RACbnHAK4PXXurVJYIXK6Va5qrZLLd7iyd3vLmSTSqweQ130_provenance.
- NP208296.RACbnHAK4PXXurVJYIXK6Va5qrZLLd7iyd3vLmSTSqweQ130_assertion evidence source_evidence_literature NP208296.RACbnHAK4PXXurVJYIXK6Va5qrZLLd7iyd3vLmSTSqweQ130_provenance.
- NP208296.RACbnHAK4PXXurVJYIXK6Va5qrZLLd7iyd3vLmSTSqweQ130_assertion SIO_000772 16125992 NP208296.RACbnHAK4PXXurVJYIXK6Va5qrZLLd7iyd3vLmSTSqweQ130_provenance.
- NP208296.RACbnHAK4PXXurVJYIXK6Va5qrZLLd7iyd3vLmSTSqweQ130_assertion wasDerivedFrom befree-20140225 NP208296.RACbnHAK4PXXurVJYIXK6Va5qrZLLd7iyd3vLmSTSqweQ130_provenance.
- NP208296.RACbnHAK4PXXurVJYIXK6Va5qrZLLd7iyd3vLmSTSqweQ130_assertion wasGeneratedBy ECO_0000203 NP208296.RACbnHAK4PXXurVJYIXK6Va5qrZLLd7iyd3vLmSTSqweQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP208296.RACbnHAK4PXXurVJYIXK6Va5qrZLLd7iyd3vLmSTSqweQ130_provenance.