Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP499319.RAwSwG9Bo25RQhPB--A0fshBXiBha_T2d8L89i-PjgiD0130_assertion> ?p ?o ?g. }
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- NP499319.RAwSwG9Bo25RQhPB--A0fshBXiBha_T2d8L89i-PjgiD0130_assertion type Assertion NP499319.RAwSwG9Bo25RQhPB--A0fshBXiBha_T2d8L89i-PjgiD0130_head.
- NP499319.RAwSwG9Bo25RQhPB--A0fshBXiBha_T2d8L89i-PjgiD0130_assertion description "[Recent studies have demonstrated that the hCHK2 1100delC mutation acts as a low-penetrance tumour suppressor gene in familial breast cancer not associated with mutations in BRCA1 or BRCA2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499319.RAwSwG9Bo25RQhPB--A0fshBXiBha_T2d8L89i-PjgiD0130_provenance.
- NP499319.RAwSwG9Bo25RQhPB--A0fshBXiBha_T2d8L89i-PjgiD0130_assertion evidence source_evidence_literature NP499319.RAwSwG9Bo25RQhPB--A0fshBXiBha_T2d8L89i-PjgiD0130_provenance.
- NP499319.RAwSwG9Bo25RQhPB--A0fshBXiBha_T2d8L89i-PjgiD0130_assertion SIO_000772 12793891 NP499319.RAwSwG9Bo25RQhPB--A0fshBXiBha_T2d8L89i-PjgiD0130_provenance.
- NP499319.RAwSwG9Bo25RQhPB--A0fshBXiBha_T2d8L89i-PjgiD0130_assertion wasDerivedFrom befree-20140225 NP499319.RAwSwG9Bo25RQhPB--A0fshBXiBha_T2d8L89i-PjgiD0130_provenance.
- NP499319.RAwSwG9Bo25RQhPB--A0fshBXiBha_T2d8L89i-PjgiD0130_assertion wasGeneratedBy ECO_0000203 NP499319.RAwSwG9Bo25RQhPB--A0fshBXiBha_T2d8L89i-PjgiD0130_provenance.