Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP782444.RADtxjiLGD3CAYvkvfr67je45Bt-knY-CLw_7gyo21JUI130_assertion> ?p ?o ?g. }
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- NP782444.RADtxjiLGD3CAYvkvfr67je45Bt-knY-CLw_7gyo21JUI130_assertion type Assertion NP782444.RADtxjiLGD3CAYvkvfr67je45Bt-knY-CLw_7gyo21JUI130_head.
- NP782444.RADtxjiLGD3CAYvkvfr67je45Bt-knY-CLw_7gyo21JUI130_assertion wasGeneratedBy ECO_0000203 NP782444.RADtxjiLGD3CAYvkvfr67je45Bt-knY-CLw_7gyo21JUI130_provenance.
- NP782444.RADtxjiLGD3CAYvkvfr67je45Bt-knY-CLw_7gyo21JUI130_assertion wasDerivedFrom befree-20150227 NP782444.RADtxjiLGD3CAYvkvfr67je45Bt-knY-CLw_7gyo21JUI130_provenance.
- NP782444.RADtxjiLGD3CAYvkvfr67je45Bt-knY-CLw_7gyo21JUI130_assertion SIO_000772 11285244 NP782444.RADtxjiLGD3CAYvkvfr67je45Bt-knY-CLw_7gyo21JUI130_provenance.
- NP782444.RADtxjiLGD3CAYvkvfr67je45Bt-knY-CLw_7gyo21JUI130_assertion evidence source_evidence_literature NP782444.RADtxjiLGD3CAYvkvfr67je45Bt-knY-CLw_7gyo21JUI130_provenance.
- NP782444.RADtxjiLGD3CAYvkvfr67je45Bt-knY-CLw_7gyo21JUI130_assertion description "[The central nervous system malformations seen in patients with ZIC2 mutations ranged from alobar HPE (most common) to middle interhemispheric fusion defect (one case).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782444.RADtxjiLGD3CAYvkvfr67je45Bt-knY-CLw_7gyo21JUI130_provenance.