Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP34667.RAugEUK0wVadhZZImxiaCb1Effh8lrr67DDgTlaKr6ERs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP34667.RAugEUK0wVadhZZImxiaCb1Effh8lrr67DDgTlaKr6ERs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP34667.RAugEUK0wVadhZZImxiaCb1Effh8lrr67DDgTlaKr6ERs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP34667.RAugEUK0wVadhZZImxiaCb1Effh8lrr67DDgTlaKr6ERs130_provenance.
- NP34667.RAugEUK0wVadhZZImxiaCb1Effh8lrr67DDgTlaKr6ERs130_assertion description "[Deep sequencing reveals 50 novel genes for recessive cognitive disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP34667.RAugEUK0wVadhZZImxiaCb1Effh8lrr67DDgTlaKr6ERs130_provenance.
- NP34667.RAugEUK0wVadhZZImxiaCb1Effh8lrr67DDgTlaKr6ERs130_assertion evidence source_evidence_curated NP34667.RAugEUK0wVadhZZImxiaCb1Effh8lrr67DDgTlaKr6ERs130_provenance.
- NP34667.RAugEUK0wVadhZZImxiaCb1Effh8lrr67DDgTlaKr6ERs130_assertion SIO_000772 21937992 NP34667.RAugEUK0wVadhZZImxiaCb1Effh8lrr67DDgTlaKr6ERs130_provenance.
- NP34667.RAugEUK0wVadhZZImxiaCb1Effh8lrr67DDgTlaKr6ERs130_assertion wasDerivedFrom ctd_human-20150221 NP34667.RAugEUK0wVadhZZImxiaCb1Effh8lrr67DDgTlaKr6ERs130_provenance.
- NP34667.RAugEUK0wVadhZZImxiaCb1Effh8lrr67DDgTlaKr6ERs130_assertion wasGeneratedBy ECO_0000218 NP34667.RAugEUK0wVadhZZImxiaCb1Effh8lrr67DDgTlaKr6ERs130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP34667.RAugEUK0wVadhZZImxiaCb1Effh8lrr67DDgTlaKr6ERs130_provenance.