Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP533236.RA8HeybfgNNW_WrZEGnAjSe0DmJIqc0P1xzDtWmvzAoic130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP533236.RA8HeybfgNNW_WrZEGnAjSe0DmJIqc0P1xzDtWmvzAoic130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP533236.RA8HeybfgNNW_WrZEGnAjSe0DmJIqc0P1xzDtWmvzAoic130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP533236.RA8HeybfgNNW_WrZEGnAjSe0DmJIqc0P1xzDtWmvzAoic130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP533236.RA8HeybfgNNW_WrZEGnAjSe0DmJIqc0P1xzDtWmvzAoic130_provenance.