Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP234030.RAlV30cVGE22n8cRLpitg30bW94DWoWJWEJp-YnHJR9p8130_assertion> ?p ?o ?g. }
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- NP234030.RAlV30cVGE22n8cRLpitg30bW94DWoWJWEJp-YnHJR9p8130_assertion type Assertion NP234030.RAlV30cVGE22n8cRLpitg30bW94DWoWJWEJp-YnHJR9p8130_head.
- NP234030.RAlV30cVGE22n8cRLpitg30bW94DWoWJWEJp-YnHJR9p8130_assertion description "[The lack of BRCA1 mutations in exon 11 which represents 61% of the entire coding sequence may provide additional insight into BRCA1 associated breast and ovarian tumor development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP234030.RAlV30cVGE22n8cRLpitg30bW94DWoWJWEJp-YnHJR9p8130_provenance.
- NP234030.RAlV30cVGE22n8cRLpitg30bW94DWoWJWEJp-YnHJR9p8130_assertion evidence source_evidence_literature NP234030.RAlV30cVGE22n8cRLpitg30bW94DWoWJWEJp-YnHJR9p8130_provenance.
- NP234030.RAlV30cVGE22n8cRLpitg30bW94DWoWJWEJp-YnHJR9p8130_assertion SIO_000772 9115962 NP234030.RAlV30cVGE22n8cRLpitg30bW94DWoWJWEJp-YnHJR9p8130_provenance.
- NP234030.RAlV30cVGE22n8cRLpitg30bW94DWoWJWEJp-YnHJR9p8130_assertion wasDerivedFrom befree-20140225 NP234030.RAlV30cVGE22n8cRLpitg30bW94DWoWJWEJp-YnHJR9p8130_provenance.
- NP234030.RAlV30cVGE22n8cRLpitg30bW94DWoWJWEJp-YnHJR9p8130_assertion wasGeneratedBy ECO_0000203 NP234030.RAlV30cVGE22n8cRLpitg30bW94DWoWJWEJp-YnHJR9p8130_provenance.