Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP916496.RA-7_mxrudErQ_QCHs11eDaAeyeXrmW13ziOFdwCeZsmc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP916496.RA-7_mxrudErQ_QCHs11eDaAeyeXrmW13ziOFdwCeZsmc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP916496.RA-7_mxrudErQ_QCHs11eDaAeyeXrmW13ziOFdwCeZsmc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP916496.RA-7_mxrudErQ_QCHs11eDaAeyeXrmW13ziOFdwCeZsmc130_provenance.
- NP916496.RA-7_mxrudErQ_QCHs11eDaAeyeXrmW13ziOFdwCeZsmc130_assertion description "[We report an infant with holoprosencephaly (HPE), sacral anomalies, and situs ambiguus with a 46,XY,der(7)t(2;7)(p23.2;q36.1) karyotype as a result of an adjacent-1 segregation of a t(2;7)pat.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916496.RA-7_mxrudErQ_QCHs11eDaAeyeXrmW13ziOFdwCeZsmc130_provenance.
- NP916496.RA-7_mxrudErQ_QCHs11eDaAeyeXrmW13ziOFdwCeZsmc130_assertion evidence source_evidence_literature NP916496.RA-7_mxrudErQ_QCHs11eDaAeyeXrmW13ziOFdwCeZsmc130_provenance.
- NP916496.RA-7_mxrudErQ_QCHs11eDaAeyeXrmW13ziOFdwCeZsmc130_assertion SIO_000772 10852374 NP916496.RA-7_mxrudErQ_QCHs11eDaAeyeXrmW13ziOFdwCeZsmc130_provenance.
- NP916496.RA-7_mxrudErQ_QCHs11eDaAeyeXrmW13ziOFdwCeZsmc130_assertion wasDerivedFrom befree-20140225 NP916496.RA-7_mxrudErQ_QCHs11eDaAeyeXrmW13ziOFdwCeZsmc130_provenance.
- NP916496.RA-7_mxrudErQ_QCHs11eDaAeyeXrmW13ziOFdwCeZsmc130_assertion wasGeneratedBy ECO_0000203 NP916496.RA-7_mxrudErQ_QCHs11eDaAeyeXrmW13ziOFdwCeZsmc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP916496.RA-7_mxrudErQ_QCHs11eDaAeyeXrmW13ziOFdwCeZsmc130_provenance.