Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418372.RAc_od4omegem8msE7VN3znr9Sd9dkr8El_hQZUF2mpPQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418372.RAc_od4omegem8msE7VN3znr9Sd9dkr8El_hQZUF2mpPQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418372.RAc_od4omegem8msE7VN3znr9Sd9dkr8El_hQZUF2mpPQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418372.RAc_od4omegem8msE7VN3znr9Sd9dkr8El_hQZUF2mpPQ130_provenance.
- NP418372.RAc_od4omegem8msE7VN3znr9Sd9dkr8El_hQZUF2mpPQ130_assertion description "[Recently, a mutation in the pantothenate kinase (PANK2) gene on band 20pl3 has been described in patients with typical HSD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418372.RAc_od4omegem8msE7VN3znr9Sd9dkr8El_hQZUF2mpPQ130_provenance.
- NP418372.RAc_od4omegem8msE7VN3znr9Sd9dkr8El_hQZUF2mpPQ130_assertion evidence source_evidence_literature NP418372.RAc_od4omegem8msE7VN3znr9Sd9dkr8El_hQZUF2mpPQ130_provenance.
- NP418372.RAc_od4omegem8msE7VN3znr9Sd9dkr8El_hQZUF2mpPQ130_assertion SIO_000772 14580665 NP418372.RAc_od4omegem8msE7VN3znr9Sd9dkr8El_hQZUF2mpPQ130_provenance.
- NP418372.RAc_od4omegem8msE7VN3znr9Sd9dkr8El_hQZUF2mpPQ130_assertion wasDerivedFrom befree-2016 NP418372.RAc_od4omegem8msE7VN3znr9Sd9dkr8El_hQZUF2mpPQ130_provenance.
- NP418372.RAc_od4omegem8msE7VN3znr9Sd9dkr8El_hQZUF2mpPQ130_assertion wasGeneratedBy ECO_0000203 NP418372.RAc_od4omegem8msE7VN3znr9Sd9dkr8El_hQZUF2mpPQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP418372.RAc_od4omegem8msE7VN3znr9Sd9dkr8El_hQZUF2mpPQ130_provenance.