Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP822470.RARJY2AXj3g9310viTf8w5QKTLpKkSR7kY7D7I1NPwFJk130_assertion> ?p ?o ?g. }
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- NP822470.RARJY2AXj3g9310viTf8w5QKTLpKkSR7kY7D7I1NPwFJk130_assertion type Assertion NP822470.RARJY2AXj3g9310viTf8w5QKTLpKkSR7kY7D7I1NPwFJk130_head.
- NP822470.RARJY2AXj3g9310viTf8w5QKTLpKkSR7kY7D7I1NPwFJk130_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." NP822470.RARJY2AXj3g9310viTf8w5QKTLpKkSR7kY7D7I1NPwFJk130_provenance.
- NP822470.RARJY2AXj3g9310viTf8w5QKTLpKkSR7kY7D7I1NPwFJk130_assertion evidence source_evidence_literature NP822470.RARJY2AXj3g9310viTf8w5QKTLpKkSR7kY7D7I1NPwFJk130_provenance.
- NP822470.RARJY2AXj3g9310viTf8w5QKTLpKkSR7kY7D7I1NPwFJk130_assertion SIO_000772 16246145 NP822470.RARJY2AXj3g9310viTf8w5QKTLpKkSR7kY7D7I1NPwFJk130_provenance.
- NP822470.RARJY2AXj3g9310viTf8w5QKTLpKkSR7kY7D7I1NPwFJk130_assertion wasDerivedFrom befree-20150227 NP822470.RARJY2AXj3g9310viTf8w5QKTLpKkSR7kY7D7I1NPwFJk130_provenance.
- NP822470.RARJY2AXj3g9310viTf8w5QKTLpKkSR7kY7D7I1NPwFJk130_assertion wasGeneratedBy ECO_0000203 NP822470.RARJY2AXj3g9310viTf8w5QKTLpKkSR7kY7D7I1NPwFJk130_provenance.