Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP208296.RACbnHAK4PXXurVJYIXK6Va5qrZLLd7iyd3vLmSTSqweQ130_assertion> ?p ?o ?g. }
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- NP208296.RACbnHAK4PXXurVJYIXK6Va5qrZLLd7iyd3vLmSTSqweQ130_assertion type Assertion NP208296.RACbnHAK4PXXurVJYIXK6Va5qrZLLd7iyd3vLmSTSqweQ130_head.
- 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.