Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP343115.RAvaFaHwBJVF-eLUhFg3ImfU46o5nsYyfEOMlFCDdEhEs130_assertion> ?p ?o ?g. }
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- NP343115.RAvaFaHwBJVF-eLUhFg3ImfU46o5nsYyfEOMlFCDdEhEs130_assertion type Assertion NP343115.RAvaFaHwBJVF-eLUhFg3ImfU46o5nsYyfEOMlFCDdEhEs130_head.
- NP343115.RAvaFaHwBJVF-eLUhFg3ImfU46o5nsYyfEOMlFCDdEhEs130_assertion description "[Here, in an individual, we demonstrate that a homozygous novel mutation in the MMR gene MSH2 is associated with leukemia and multiple caf�-au-lait spots, a feature of neurofibromatosis type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343115.RAvaFaHwBJVF-eLUhFg3ImfU46o5nsYyfEOMlFCDdEhEs130_provenance.
- NP343115.RAvaFaHwBJVF-eLUhFg3ImfU46o5nsYyfEOMlFCDdEhEs130_assertion evidence source_evidence_literature NP343115.RAvaFaHwBJVF-eLUhFg3ImfU46o5nsYyfEOMlFCDdEhEs130_provenance.
- NP343115.RAvaFaHwBJVF-eLUhFg3ImfU46o5nsYyfEOMlFCDdEhEs130_assertion SIO_000772 11809679 NP343115.RAvaFaHwBJVF-eLUhFg3ImfU46o5nsYyfEOMlFCDdEhEs130_provenance.
- NP343115.RAvaFaHwBJVF-eLUhFg3ImfU46o5nsYyfEOMlFCDdEhEs130_assertion wasDerivedFrom befree-2016 NP343115.RAvaFaHwBJVF-eLUhFg3ImfU46o5nsYyfEOMlFCDdEhEs130_provenance.
- NP343115.RAvaFaHwBJVF-eLUhFg3ImfU46o5nsYyfEOMlFCDdEhEs130_assertion wasGeneratedBy ECO_0000203 NP343115.RAvaFaHwBJVF-eLUhFg3ImfU46o5nsYyfEOMlFCDdEhEs130_provenance.