Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP763329.RA4t-6rjl2qzrdd4F9C-KHD3cdYbBbxiuNpnvojpVdxIY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP763329.RA4t-6rjl2qzrdd4F9C-KHD3cdYbBbxiuNpnvojpVdxIY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP763329.RA4t-6rjl2qzrdd4F9C-KHD3cdYbBbxiuNpnvojpVdxIY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP763329.RA4t-6rjl2qzrdd4F9C-KHD3cdYbBbxiuNpnvojpVdxIY130_provenance.
- NP763329.RA4t-6rjl2qzrdd4F9C-KHD3cdYbBbxiuNpnvojpVdxIY130_assertion description "[Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763329.RA4t-6rjl2qzrdd4F9C-KHD3cdYbBbxiuNpnvojpVdxIY130_provenance.
- NP763329.RA4t-6rjl2qzrdd4F9C-KHD3cdYbBbxiuNpnvojpVdxIY130_assertion evidence source_evidence_literature NP763329.RA4t-6rjl2qzrdd4F9C-KHD3cdYbBbxiuNpnvojpVdxIY130_provenance.
- NP763329.RA4t-6rjl2qzrdd4F9C-KHD3cdYbBbxiuNpnvojpVdxIY130_assertion SIO_000772 17941886 NP763329.RA4t-6rjl2qzrdd4F9C-KHD3cdYbBbxiuNpnvojpVdxIY130_provenance.
- NP763329.RA4t-6rjl2qzrdd4F9C-KHD3cdYbBbxiuNpnvojpVdxIY130_assertion wasDerivedFrom befree-20140225 NP763329.RA4t-6rjl2qzrdd4F9C-KHD3cdYbBbxiuNpnvojpVdxIY130_provenance.
- NP763329.RA4t-6rjl2qzrdd4F9C-KHD3cdYbBbxiuNpnvojpVdxIY130_assertion wasGeneratedBy ECO_0000203 NP763329.RA4t-6rjl2qzrdd4F9C-KHD3cdYbBbxiuNpnvojpVdxIY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP763329.RA4t-6rjl2qzrdd4F9C-KHD3cdYbBbxiuNpnvojpVdxIY130_provenance.