Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP435632.RASjl2Hg19Dj4mmIowEkv8keDTJ1Pth8sZmW3dNu2-Fws130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP435632.RASjl2Hg19Dj4mmIowEkv8keDTJ1Pth8sZmW3dNu2-Fws130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP435632.RASjl2Hg19Dj4mmIowEkv8keDTJ1Pth8sZmW3dNu2-Fws130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP435632.RASjl2Hg19Dj4mmIowEkv8keDTJ1Pth8sZmW3dNu2-Fws130_provenance.
- NP435632.RASjl2Hg19Dj4mmIowEkv8keDTJ1Pth8sZmW3dNu2-Fws130_assertion description "[Split hand/foot malformation type I (SHFM1) disease locus maps to chromosome 7q21.3-q22, a region that includes the distal-less-related (dll) genes DLX5 and DLX6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435632.RASjl2Hg19Dj4mmIowEkv8keDTJ1Pth8sZmW3dNu2-Fws130_provenance.
- NP435632.RASjl2Hg19Dj4mmIowEkv8keDTJ1Pth8sZmW3dNu2-Fws130_assertion evidence source_evidence_literature NP435632.RASjl2Hg19Dj4mmIowEkv8keDTJ1Pth8sZmW3dNu2-Fws130_provenance.
- NP435632.RASjl2Hg19Dj4mmIowEkv8keDTJ1Pth8sZmW3dNu2-Fws130_assertion SIO_000772 12112878 NP435632.RASjl2Hg19Dj4mmIowEkv8keDTJ1Pth8sZmW3dNu2-Fws130_provenance.
- NP435632.RASjl2Hg19Dj4mmIowEkv8keDTJ1Pth8sZmW3dNu2-Fws130_assertion wasDerivedFrom befree-20140225 NP435632.RASjl2Hg19Dj4mmIowEkv8keDTJ1Pth8sZmW3dNu2-Fws130_provenance.
- NP435632.RASjl2Hg19Dj4mmIowEkv8keDTJ1Pth8sZmW3dNu2-Fws130_assertion wasGeneratedBy ECO_0000203 NP435632.RASjl2Hg19Dj4mmIowEkv8keDTJ1Pth8sZmW3dNu2-Fws130_provenance.
- befree-20140225 importedOn "2014-02-25" NP435632.RASjl2Hg19Dj4mmIowEkv8keDTJ1Pth8sZmW3dNu2-Fws130_provenance.