Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP676275.RALf58xzgGQc6hBxjEMWzChMZ-ghPgVSvWV9D-ts7XBrs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP676275.RALf58xzgGQc6hBxjEMWzChMZ-ghPgVSvWV9D-ts7XBrs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP676275.RALf58xzgGQc6hBxjEMWzChMZ-ghPgVSvWV9D-ts7XBrs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP676275.RALf58xzgGQc6hBxjEMWzChMZ-ghPgVSvWV9D-ts7XBrs130_provenance.
- NP676275.RALf58xzgGQc6hBxjEMWzChMZ-ghPgVSvWV9D-ts7XBrs130_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." NP676275.RALf58xzgGQc6hBxjEMWzChMZ-ghPgVSvWV9D-ts7XBrs130_provenance.
- NP676275.RALf58xzgGQc6hBxjEMWzChMZ-ghPgVSvWV9D-ts7XBrs130_assertion evidence source_evidence_literature NP676275.RALf58xzgGQc6hBxjEMWzChMZ-ghPgVSvWV9D-ts7XBrs130_provenance.
- NP676275.RALf58xzgGQc6hBxjEMWzChMZ-ghPgVSvWV9D-ts7XBrs130_assertion SIO_000772 23283079 NP676275.RALf58xzgGQc6hBxjEMWzChMZ-ghPgVSvWV9D-ts7XBrs130_provenance.
- NP676275.RALf58xzgGQc6hBxjEMWzChMZ-ghPgVSvWV9D-ts7XBrs130_assertion wasDerivedFrom befree-20140225 NP676275.RALf58xzgGQc6hBxjEMWzChMZ-ghPgVSvWV9D-ts7XBrs130_provenance.
- NP676275.RALf58xzgGQc6hBxjEMWzChMZ-ghPgVSvWV9D-ts7XBrs130_assertion wasGeneratedBy ECO_0000203 NP676275.RALf58xzgGQc6hBxjEMWzChMZ-ghPgVSvWV9D-ts7XBrs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP676275.RALf58xzgGQc6hBxjEMWzChMZ-ghPgVSvWV9D-ts7XBrs130_provenance.