Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP21206.RAspioKgzNuVLLoo2bkkVF9DTmb6l2enWgkIsgJgoZwgg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP21206.RAspioKgzNuVLLoo2bkkVF9DTmb6l2enWgkIsgJgoZwgg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP21206.RAspioKgzNuVLLoo2bkkVF9DTmb6l2enWgkIsgJgoZwgg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP21206.RAspioKgzNuVLLoo2bkkVF9DTmb6l2enWgkIsgJgoZwgg130_provenance.
- NP21206.RAspioKgzNuVLLoo2bkkVF9DTmb6l2enWgkIsgJgoZwgg130_assertion description "[Two patients with balanced translocations and autistic disorder: CSMD3 as a candidate gene for autism found in their common 8q23 breakpoint area.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP21206.RAspioKgzNuVLLoo2bkkVF9DTmb6l2enWgkIsgJgoZwgg130_provenance.
- NP21206.RAspioKgzNuVLLoo2bkkVF9DTmb6l2enWgkIsgJgoZwgg130_assertion evidence source_evidence_curated NP21206.RAspioKgzNuVLLoo2bkkVF9DTmb6l2enWgkIsgJgoZwgg130_provenance.
- NP21206.RAspioKgzNuVLLoo2bkkVF9DTmb6l2enWgkIsgJgoZwgg130_assertion SIO_000772 18270536 NP21206.RAspioKgzNuVLLoo2bkkVF9DTmb6l2enWgkIsgJgoZwgg130_provenance.
- NP21206.RAspioKgzNuVLLoo2bkkVF9DTmb6l2enWgkIsgJgoZwgg130_assertion wasDerivedFrom ctd_human-2016 NP21206.RAspioKgzNuVLLoo2bkkVF9DTmb6l2enWgkIsgJgoZwgg130_provenance.
- NP21206.RAspioKgzNuVLLoo2bkkVF9DTmb6l2enWgkIsgJgoZwgg130_assertion wasGeneratedBy ECO_0000218 NP21206.RAspioKgzNuVLLoo2bkkVF9DTmb6l2enWgkIsgJgoZwgg130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP21206.RAspioKgzNuVLLoo2bkkVF9DTmb6l2enWgkIsgJgoZwgg130_provenance.