Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP883.RAxpHgLNwc33ZgrzrGZdkitDHGP1EKRUDJ5X8q35-ckT8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP883.RAxpHgLNwc33ZgrzrGZdkitDHGP1EKRUDJ5X8q35-ckT8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP883.RAxpHgLNwc33ZgrzrGZdkitDHGP1EKRUDJ5X8q35-ckT8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP883.RAxpHgLNwc33ZgrzrGZdkitDHGP1EKRUDJ5X8q35-ckT8130_provenance.
- NP883.RAxpHgLNwc33ZgrzrGZdkitDHGP1EKRUDJ5X8q35-ckT8130_assertion description "[Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP883.RAxpHgLNwc33ZgrzrGZdkitDHGP1EKRUDJ5X8q35-ckT8130_provenance.
- NP883.RAxpHgLNwc33ZgrzrGZdkitDHGP1EKRUDJ5X8q35-ckT8130_assertion evidence source_evidence_curated NP883.RAxpHgLNwc33ZgrzrGZdkitDHGP1EKRUDJ5X8q35-ckT8130_provenance.
- NP883.RAxpHgLNwc33ZgrzrGZdkitDHGP1EKRUDJ5X8q35-ckT8130_assertion SIO_000772 10762541 NP883.RAxpHgLNwc33ZgrzrGZdkitDHGP1EKRUDJ5X8q35-ckT8130_provenance.
- NP883.RAxpHgLNwc33ZgrzrGZdkitDHGP1EKRUDJ5X8q35-ckT8130_assertion wasDerivedFrom uniprot-20130724 NP883.RAxpHgLNwc33ZgrzrGZdkitDHGP1EKRUDJ5X8q35-ckT8130_provenance.
- NP883.RAxpHgLNwc33ZgrzrGZdkitDHGP1EKRUDJ5X8q35-ckT8130_assertion wasGeneratedBy ECO_0000218 NP883.RAxpHgLNwc33ZgrzrGZdkitDHGP1EKRUDJ5X8q35-ckT8130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP883.RAxpHgLNwc33ZgrzrGZdkitDHGP1EKRUDJ5X8q35-ckT8130_provenance.