Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP519271.RAByStMP-68eKUw0FOs25PDKXm0Nu7yEK224sYvP2neg0130_assertion> ?p ?o ?g. }
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- NP519271.RAByStMP-68eKUw0FOs25PDKXm0Nu7yEK224sYvP2neg0130_assertion type Assertion NP519271.RAByStMP-68eKUw0FOs25PDKXm0Nu7yEK224sYvP2neg0130_head.
- NP519271.RAByStMP-68eKUw0FOs25PDKXm0Nu7yEK224sYvP2neg0130_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." NP519271.RAByStMP-68eKUw0FOs25PDKXm0Nu7yEK224sYvP2neg0130_provenance.
- NP519271.RAByStMP-68eKUw0FOs25PDKXm0Nu7yEK224sYvP2neg0130_assertion evidence source_evidence_literature NP519271.RAByStMP-68eKUw0FOs25PDKXm0Nu7yEK224sYvP2neg0130_provenance.
- NP519271.RAByStMP-68eKUw0FOs25PDKXm0Nu7yEK224sYvP2neg0130_assertion SIO_000772 16246145 NP519271.RAByStMP-68eKUw0FOs25PDKXm0Nu7yEK224sYvP2neg0130_provenance.
- NP519271.RAByStMP-68eKUw0FOs25PDKXm0Nu7yEK224sYvP2neg0130_assertion wasDerivedFrom befree-2016 NP519271.RAByStMP-68eKUw0FOs25PDKXm0Nu7yEK224sYvP2neg0130_provenance.
- NP519271.RAByStMP-68eKUw0FOs25PDKXm0Nu7yEK224sYvP2neg0130_assertion wasGeneratedBy ECO_0000203 NP519271.RAByStMP-68eKUw0FOs25PDKXm0Nu7yEK224sYvP2neg0130_provenance.