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- source_evidence_literature type ECO_0000212 NP753310.RAUa7Fcl3N-8wEuvGX50L9_wokDqHnTqYAUgJlKetqEWE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP753310.RAUa7Fcl3N-8wEuvGX50L9_wokDqHnTqYAUgJlKetqEWE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP753310.RAUa7Fcl3N-8wEuvGX50L9_wokDqHnTqYAUgJlKetqEWE130_provenance.
- NP753310.RAUa7Fcl3N-8wEuvGX50L9_wokDqHnTqYAUgJlKetqEWE130_assertion description "[Recently, mutations in the CRTAP and LEPRE1 genes were found to cause some rare forms of human OI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP753310.RAUa7Fcl3N-8wEuvGX50L9_wokDqHnTqYAUgJlKetqEWE130_provenance.
- NP753310.RAUa7Fcl3N-8wEuvGX50L9_wokDqHnTqYAUgJlKetqEWE130_assertion evidence source_evidence_literature NP753310.RAUa7Fcl3N-8wEuvGX50L9_wokDqHnTqYAUgJlKetqEWE130_provenance.
- NP753310.RAUa7Fcl3N-8wEuvGX50L9_wokDqHnTqYAUgJlKetqEWE130_assertion SIO_000772 19629171 NP753310.RAUa7Fcl3N-8wEuvGX50L9_wokDqHnTqYAUgJlKetqEWE130_provenance.
- NP753310.RAUa7Fcl3N-8wEuvGX50L9_wokDqHnTqYAUgJlKetqEWE130_assertion wasDerivedFrom befree-2016 NP753310.RAUa7Fcl3N-8wEuvGX50L9_wokDqHnTqYAUgJlKetqEWE130_provenance.
- NP753310.RAUa7Fcl3N-8wEuvGX50L9_wokDqHnTqYAUgJlKetqEWE130_assertion wasGeneratedBy ECO_0000203 NP753310.RAUa7Fcl3N-8wEuvGX50L9_wokDqHnTqYAUgJlKetqEWE130_provenance.
- befree-2016 importedOn "2016-02-19" NP753310.RAUa7Fcl3N-8wEuvGX50L9_wokDqHnTqYAUgJlKetqEWE130_provenance.