Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_provenance.
- NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_assertion description "[Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_provenance.
- NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_assertion evidence source_evidence_literature NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_provenance.
- NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_assertion SIO_000772 19221116 NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_provenance.
- NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_assertion wasDerivedFrom gad-20150221 NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_provenance.
- NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_assertion wasGeneratedBy ECO_0000203 NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_provenance.