Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6903.RASqiBW9MYf6TZzmXAQah1FFrsfFsjb3UVsBZ3iCnbtUA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6903.RASqiBW9MYf6TZzmXAQah1FFrsfFsjb3UVsBZ3iCnbtUA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6903.RASqiBW9MYf6TZzmXAQah1FFrsfFsjb3UVsBZ3iCnbtUA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6903.RASqiBW9MYf6TZzmXAQah1FFrsfFsjb3UVsBZ3iCnbtUA130_provenance.
- NP6903.RASqiBW9MYf6TZzmXAQah1FFrsfFsjb3UVsBZ3iCnbtUA130_assertion description "[Structural variation of chromosomes in autism spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6903.RASqiBW9MYf6TZzmXAQah1FFrsfFsjb3UVsBZ3iCnbtUA130_provenance.
- NP6903.RASqiBW9MYf6TZzmXAQah1FFrsfFsjb3UVsBZ3iCnbtUA130_assertion evidence source_evidence_curated NP6903.RASqiBW9MYf6TZzmXAQah1FFrsfFsjb3UVsBZ3iCnbtUA130_provenance.
- NP6903.RASqiBW9MYf6TZzmXAQah1FFrsfFsjb3UVsBZ3iCnbtUA130_assertion SIO_000772 18252227 NP6903.RASqiBW9MYf6TZzmXAQah1FFrsfFsjb3UVsBZ3iCnbtUA130_provenance.
- NP6903.RASqiBW9MYf6TZzmXAQah1FFrsfFsjb3UVsBZ3iCnbtUA130_assertion wasDerivedFrom ctd_human-20150221 NP6903.RASqiBW9MYf6TZzmXAQah1FFrsfFsjb3UVsBZ3iCnbtUA130_provenance.
- NP6903.RASqiBW9MYf6TZzmXAQah1FFrsfFsjb3UVsBZ3iCnbtUA130_assertion wasGeneratedBy ECO_0000218 NP6903.RASqiBW9MYf6TZzmXAQah1FFrsfFsjb3UVsBZ3iCnbtUA130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP6903.RASqiBW9MYf6TZzmXAQah1FFrsfFsjb3UVsBZ3iCnbtUA130_provenance.