Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP533236.RA8HeybfgNNW_WrZEGnAjSe0DmJIqc0P1xzDtWmvzAoic130_assertion> ?p ?o ?g. }
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- NP533236.RA8HeybfgNNW_WrZEGnAjSe0DmJIqc0P1xzDtWmvzAoic130_assertion type Assertion NP533236.RA8HeybfgNNW_WrZEGnAjSe0DmJIqc0P1xzDtWmvzAoic130_head.
- NP533236.RA8HeybfgNNW_WrZEGnAjSe0DmJIqc0P1xzDtWmvzAoic130_assertion description "[Here we report a sporadic patient with SHFLD who carries a de novo chromosomal translocation t(2;18)(q14.2;p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP533236.RA8HeybfgNNW_WrZEGnAjSe0DmJIqc0P1xzDtWmvzAoic130_provenance.
- NP533236.RA8HeybfgNNW_WrZEGnAjSe0DmJIqc0P1xzDtWmvzAoic130_assertion evidence source_evidence_literature NP533236.RA8HeybfgNNW_WrZEGnAjSe0DmJIqc0P1xzDtWmvzAoic130_provenance.
- NP533236.RA8HeybfgNNW_WrZEGnAjSe0DmJIqc0P1xzDtWmvzAoic130_assertion SIO_000772 17569090 NP533236.RA8HeybfgNNW_WrZEGnAjSe0DmJIqc0P1xzDtWmvzAoic130_provenance.
- NP533236.RA8HeybfgNNW_WrZEGnAjSe0DmJIqc0P1xzDtWmvzAoic130_assertion wasDerivedFrom befree-20140225 NP533236.RA8HeybfgNNW_WrZEGnAjSe0DmJIqc0P1xzDtWmvzAoic130_provenance.
- NP533236.RA8HeybfgNNW_WrZEGnAjSe0DmJIqc0P1xzDtWmvzAoic130_assertion wasGeneratedBy ECO_0000203 NP533236.RA8HeybfgNNW_WrZEGnAjSe0DmJIqc0P1xzDtWmvzAoic130_provenance.