Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP23222.RAanco1N5xK6R4DYVX7_cZIAWB_zjT6twGinM1yf1dIOg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP23222.RAanco1N5xK6R4DYVX7_cZIAWB_zjT6twGinM1yf1dIOg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP23222.RAanco1N5xK6R4DYVX7_cZIAWB_zjT6twGinM1yf1dIOg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP23222.RAanco1N5xK6R4DYVX7_cZIAWB_zjT6twGinM1yf1dIOg130_provenance.
- NP23222.RAanco1N5xK6R4DYVX7_cZIAWB_zjT6twGinM1yf1dIOg130_assertion description "[DCTN1 mutations in Perry syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP23222.RAanco1N5xK6R4DYVX7_cZIAWB_zjT6twGinM1yf1dIOg130_provenance.
- NP23222.RAanco1N5xK6R4DYVX7_cZIAWB_zjT6twGinM1yf1dIOg130_assertion evidence source_evidence_curated NP23222.RAanco1N5xK6R4DYVX7_cZIAWB_zjT6twGinM1yf1dIOg130_provenance.
- NP23222.RAanco1N5xK6R4DYVX7_cZIAWB_zjT6twGinM1yf1dIOg130_assertion SIO_000772 19136952 NP23222.RAanco1N5xK6R4DYVX7_cZIAWB_zjT6twGinM1yf1dIOg130_provenance.
- NP23222.RAanco1N5xK6R4DYVX7_cZIAWB_zjT6twGinM1yf1dIOg130_assertion wasDerivedFrom ctd_human-2016 NP23222.RAanco1N5xK6R4DYVX7_cZIAWB_zjT6twGinM1yf1dIOg130_provenance.
- NP23222.RAanco1N5xK6R4DYVX7_cZIAWB_zjT6twGinM1yf1dIOg130_assertion wasGeneratedBy ECO_0000218 NP23222.RAanco1N5xK6R4DYVX7_cZIAWB_zjT6twGinM1yf1dIOg130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP23222.RAanco1N5xK6R4DYVX7_cZIAWB_zjT6twGinM1yf1dIOg130_provenance.