Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP879800.RAn9bBUIEikbiaqvq8DEff7m9OgO78XSOfrCbPE-ikbrU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP879800.RAn9bBUIEikbiaqvq8DEff7m9OgO78XSOfrCbPE-ikbrU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP879800.RAn9bBUIEikbiaqvq8DEff7m9OgO78XSOfrCbPE-ikbrU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP879800.RAn9bBUIEikbiaqvq8DEff7m9OgO78XSOfrCbPE-ikbrU130_provenance.
- NP879800.RAn9bBUIEikbiaqvq8DEff7m9OgO78XSOfrCbPE-ikbrU130_assertion description "[An MKS-like incipient congenic group (F6 to F10) manifested very variable neurological features (including exencephaly, and frontal/occipital encephalocele) that were associated with the loss of primary cilia, diminished Shh signalling and dorsalization of the caudal neural tube.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP879800.RAn9bBUIEikbiaqvq8DEff7m9OgO78XSOfrCbPE-ikbrU130_provenance.
- NP879800.RAn9bBUIEikbiaqvq8DEff7m9OgO78XSOfrCbPE-ikbrU130_assertion evidence source_evidence_literature NP879800.RAn9bBUIEikbiaqvq8DEff7m9OgO78XSOfrCbPE-ikbrU130_provenance.
- NP879800.RAn9bBUIEikbiaqvq8DEff7m9OgO78XSOfrCbPE-ikbrU130_assertion SIO_000772 23283079 NP879800.RAn9bBUIEikbiaqvq8DEff7m9OgO78XSOfrCbPE-ikbrU130_provenance.
- NP879800.RAn9bBUIEikbiaqvq8DEff7m9OgO78XSOfrCbPE-ikbrU130_assertion wasDerivedFrom befree-20140225 NP879800.RAn9bBUIEikbiaqvq8DEff7m9OgO78XSOfrCbPE-ikbrU130_provenance.
- NP879800.RAn9bBUIEikbiaqvq8DEff7m9OgO78XSOfrCbPE-ikbrU130_assertion wasGeneratedBy ECO_0000203 NP879800.RAn9bBUIEikbiaqvq8DEff7m9OgO78XSOfrCbPE-ikbrU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP879800.RAn9bBUIEikbiaqvq8DEff7m9OgO78XSOfrCbPE-ikbrU130_provenance.