Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP553767.RA1ACdb8ETgi990Z9449QT-_c6QdzehmC73DtR8F67hSE130_assertion> ?p ?o ?g. }
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- NP553767.RA1ACdb8ETgi990Z9449QT-_c6QdzehmC73DtR8F67hSE130_assertion type Assertion NP553767.RA1ACdb8ETgi990Z9449QT-_c6QdzehmC73DtR8F67hSE130_head.
- NP553767.RA1ACdb8ETgi990Z9449QT-_c6QdzehmC73DtR8F67hSE130_assertion description "[Of the five known human RecQ family members, three (BLM, WRN and RECQ4, which cause Bloom's syndrome, Werner's syndrome and Rothmund-Thomson syndrome respectively) are mutated in distinct clinical disorders associated with cancer predisposition and/or premature aging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553767.RA1ACdb8ETgi990Z9449QT-_c6QdzehmC73DtR8F67hSE130_provenance.
- NP553767.RA1ACdb8ETgi990Z9449QT-_c6QdzehmC73DtR8F67hSE130_assertion evidence source_evidence_literature NP553767.RA1ACdb8ETgi990Z9449QT-_c6QdzehmC73DtR8F67hSE130_provenance.
- NP553767.RA1ACdb8ETgi990Z9449QT-_c6QdzehmC73DtR8F67hSE130_assertion SIO_000772 16246145 NP553767.RA1ACdb8ETgi990Z9449QT-_c6QdzehmC73DtR8F67hSE130_provenance.
- NP553767.RA1ACdb8ETgi990Z9449QT-_c6QdzehmC73DtR8F67hSE130_assertion wasDerivedFrom befree-20140225 NP553767.RA1ACdb8ETgi990Z9449QT-_c6QdzehmC73DtR8F67hSE130_provenance.
- NP553767.RA1ACdb8ETgi990Z9449QT-_c6QdzehmC73DtR8F67hSE130_assertion wasGeneratedBy ECO_0000203 NP553767.RA1ACdb8ETgi990Z9449QT-_c6QdzehmC73DtR8F67hSE130_provenance.