Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP5762.RA308t-OkYYqHYYWeAF-cpMkJ7zr4odJj6BxGmjTumHPE130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP5762.RA308t-OkYYqHYYWeAF-cpMkJ7zr4odJj6BxGmjTumHPE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5762.RA308t-OkYYqHYYWeAF-cpMkJ7zr4odJj6BxGmjTumHPE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5762.RA308t-OkYYqHYYWeAF-cpMkJ7zr4odJj6BxGmjTumHPE130_provenance.
- NP5762.RA308t-OkYYqHYYWeAF-cpMkJ7zr4odJj6BxGmjTumHPE130_assertion description "[Left-right axis malformations associated with mutations in ACVR2B, the gene for human activin receptor type IIB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5762.RA308t-OkYYqHYYWeAF-cpMkJ7zr4odJj6BxGmjTumHPE130_provenance.
- NP5762.RA308t-OkYYqHYYWeAF-cpMkJ7zr4odJj6BxGmjTumHPE130_assertion evidence source_evidence_curated NP5762.RA308t-OkYYqHYYWeAF-cpMkJ7zr4odJj6BxGmjTumHPE130_provenance.
- NP5762.RA308t-OkYYqHYYWeAF-cpMkJ7zr4odJj6BxGmjTumHPE130_assertion SIO_000772 9916847 NP5762.RA308t-OkYYqHYYWeAF-cpMkJ7zr4odJj6BxGmjTumHPE130_provenance.
- NP5762.RA308t-OkYYqHYYWeAF-cpMkJ7zr4odJj6BxGmjTumHPE130_assertion wasDerivedFrom ctd_human-20150221 NP5762.RA308t-OkYYqHYYWeAF-cpMkJ7zr4odJj6BxGmjTumHPE130_provenance.
- NP5762.RA308t-OkYYqHYYWeAF-cpMkJ7zr4odJj6BxGmjTumHPE130_assertion wasGeneratedBy ECO_0000218 NP5762.RA308t-OkYYqHYYWeAF-cpMkJ7zr4odJj6BxGmjTumHPE130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP5762.RA308t-OkYYqHYYWeAF-cpMkJ7zr4odJj6BxGmjTumHPE130_provenance.