Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP503866.RAef9IpG7tKuV8Wap-04DTf2m7qQM0-GV8sWnzdLlyeTg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP503866.RAef9IpG7tKuV8Wap-04DTf2m7qQM0-GV8sWnzdLlyeTg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP503866.RAef9IpG7tKuV8Wap-04DTf2m7qQM0-GV8sWnzdLlyeTg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP503866.RAef9IpG7tKuV8Wap-04DTf2m7qQM0-GV8sWnzdLlyeTg130_provenance.
- NP503866.RAef9IpG7tKuV8Wap-04DTf2m7qQM0-GV8sWnzdLlyeTg130_assertion description "[Our results provide a tool to a more accurate definition of Cohen syndrome(s) and a starting point for the positional cloning of CHS1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503866.RAef9IpG7tKuV8Wap-04DTf2m7qQM0-GV8sWnzdLlyeTg130_provenance.
- NP503866.RAef9IpG7tKuV8Wap-04DTf2m7qQM0-GV8sWnzdLlyeTg130_assertion evidence source_evidence_literature NP503866.RAef9IpG7tKuV8Wap-04DTf2m7qQM0-GV8sWnzdLlyeTg130_provenance.
- NP503866.RAef9IpG7tKuV8Wap-04DTf2m7qQM0-GV8sWnzdLlyeTg130_assertion SIO_000772 7920642 NP503866.RAef9IpG7tKuV8Wap-04DTf2m7qQM0-GV8sWnzdLlyeTg130_provenance.
- NP503866.RAef9IpG7tKuV8Wap-04DTf2m7qQM0-GV8sWnzdLlyeTg130_assertion wasDerivedFrom befree-20140225 NP503866.RAef9IpG7tKuV8Wap-04DTf2m7qQM0-GV8sWnzdLlyeTg130_provenance.
- NP503866.RAef9IpG7tKuV8Wap-04DTf2m7qQM0-GV8sWnzdLlyeTg130_assertion wasGeneratedBy ECO_0000203 NP503866.RAef9IpG7tKuV8Wap-04DTf2m7qQM0-GV8sWnzdLlyeTg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP503866.RAef9IpG7tKuV8Wap-04DTf2m7qQM0-GV8sWnzdLlyeTg130_provenance.