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- source_evidence_literature type ECO_0000212 NP984447.RAsUzKIYFolrRUs45MAmMkoHZu55ne_71pi1nc6M7zGcY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP984447.RAsUzKIYFolrRUs45MAmMkoHZu55ne_71pi1nc6M7zGcY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP984447.RAsUzKIYFolrRUs45MAmMkoHZu55ne_71pi1nc6M7zGcY130_provenance.
- NP984447.RAsUzKIYFolrRUs45MAmMkoHZu55ne_71pi1nc6M7zGcY130_assertion description "[Syndromic true hermaphroditism due to an R-spondin1 (RSPO1) homozygous mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP984447.RAsUzKIYFolrRUs45MAmMkoHZu55ne_71pi1nc6M7zGcY130_provenance.
- NP984447.RAsUzKIYFolrRUs45MAmMkoHZu55ne_71pi1nc6M7zGcY130_assertion evidence source_evidence_literature NP984447.RAsUzKIYFolrRUs45MAmMkoHZu55ne_71pi1nc6M7zGcY130_provenance.
- NP984447.RAsUzKIYFolrRUs45MAmMkoHZu55ne_71pi1nc6M7zGcY130_assertion SIO_000772 18085567 NP984447.RAsUzKIYFolrRUs45MAmMkoHZu55ne_71pi1nc6M7zGcY130_provenance.
- NP984447.RAsUzKIYFolrRUs45MAmMkoHZu55ne_71pi1nc6M7zGcY130_assertion wasDerivedFrom befree-20150227 NP984447.RAsUzKIYFolrRUs45MAmMkoHZu55ne_71pi1nc6M7zGcY130_provenance.
- NP984447.RAsUzKIYFolrRUs45MAmMkoHZu55ne_71pi1nc6M7zGcY130_assertion wasGeneratedBy ECO_0000203 NP984447.RAsUzKIYFolrRUs45MAmMkoHZu55ne_71pi1nc6M7zGcY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP984447.RAsUzKIYFolrRUs45MAmMkoHZu55ne_71pi1nc6M7zGcY130_provenance.