Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7465.RAeZRf2I6g7zjQUjiPec0yYC-gD3u48N5yuSibn7_GX3E130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7465.RAeZRf2I6g7zjQUjiPec0yYC-gD3u48N5yuSibn7_GX3E130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7465.RAeZRf2I6g7zjQUjiPec0yYC-gD3u48N5yuSibn7_GX3E130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7465.RAeZRf2I6g7zjQUjiPec0yYC-gD3u48N5yuSibn7_GX3E130_provenance.
- NP7465.RAeZRf2I6g7zjQUjiPec0yYC-gD3u48N5yuSibn7_GX3E130_assertion description "[ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7465.RAeZRf2I6g7zjQUjiPec0yYC-gD3u48N5yuSibn7_GX3E130_provenance.
- NP7465.RAeZRf2I6g7zjQUjiPec0yYC-gD3u48N5yuSibn7_GX3E130_assertion evidence source_evidence_curated NP7465.RAeZRf2I6g7zjQUjiPec0yYC-gD3u48N5yuSibn7_GX3E130_provenance.
- NP7465.RAeZRf2I6g7zjQUjiPec0yYC-gD3u48N5yuSibn7_GX3E130_assertion SIO_000772 23623388 NP7465.RAeZRf2I6g7zjQUjiPec0yYC-gD3u48N5yuSibn7_GX3E130_provenance.
- NP7465.RAeZRf2I6g7zjQUjiPec0yYC-gD3u48N5yuSibn7_GX3E130_assertion wasDerivedFrom uniprot-2016 NP7465.RAeZRf2I6g7zjQUjiPec0yYC-gD3u48N5yuSibn7_GX3E130_provenance.
- NP7465.RAeZRf2I6g7zjQUjiPec0yYC-gD3u48N5yuSibn7_GX3E130_assertion wasGeneratedBy ECO_0000218 NP7465.RAeZRf2I6g7zjQUjiPec0yYC-gD3u48N5yuSibn7_GX3E130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7465.RAeZRf2I6g7zjQUjiPec0yYC-gD3u48N5yuSibn7_GX3E130_provenance.