Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP7592.RAWI_Obg9FAATunMYVnFe2G-yhP9LvgLclhuUG6nHMMuw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7592.RAWI_Obg9FAATunMYVnFe2G-yhP9LvgLclhuUG6nHMMuw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7592.RAWI_Obg9FAATunMYVnFe2G-yhP9LvgLclhuUG6nHMMuw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7592.RAWI_Obg9FAATunMYVnFe2G-yhP9LvgLclhuUG6nHMMuw130_provenance.
- NP7592.RAWI_Obg9FAATunMYVnFe2G-yhP9LvgLclhuUG6nHMMuw130_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." NP7592.RAWI_Obg9FAATunMYVnFe2G-yhP9LvgLclhuUG6nHMMuw130_provenance.
- NP7592.RAWI_Obg9FAATunMYVnFe2G-yhP9LvgLclhuUG6nHMMuw130_assertion evidence source_evidence_curated NP7592.RAWI_Obg9FAATunMYVnFe2G-yhP9LvgLclhuUG6nHMMuw130_provenance.
- NP7592.RAWI_Obg9FAATunMYVnFe2G-yhP9LvgLclhuUG6nHMMuw130_assertion SIO_000772 9916847 NP7592.RAWI_Obg9FAATunMYVnFe2G-yhP9LvgLclhuUG6nHMMuw130_provenance.
- NP7592.RAWI_Obg9FAATunMYVnFe2G-yhP9LvgLclhuUG6nHMMuw130_assertion wasDerivedFrom ctd_human-20130708 NP7592.RAWI_Obg9FAATunMYVnFe2G-yhP9LvgLclhuUG6nHMMuw130_provenance.
- NP7592.RAWI_Obg9FAATunMYVnFe2G-yhP9LvgLclhuUG6nHMMuw130_assertion wasGeneratedBy ECO_0000218 NP7592.RAWI_Obg9FAATunMYVnFe2G-yhP9LvgLclhuUG6nHMMuw130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP7592.RAWI_Obg9FAATunMYVnFe2G-yhP9LvgLclhuUG6nHMMuw130_provenance.