Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP33657.RAmFmJKIXiQsNBnulfXEMF9-xpQlDovjtlnFa3ENqtkrw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP33657.RAmFmJKIXiQsNBnulfXEMF9-xpQlDovjtlnFa3ENqtkrw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP33657.RAmFmJKIXiQsNBnulfXEMF9-xpQlDovjtlnFa3ENqtkrw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP33657.RAmFmJKIXiQsNBnulfXEMF9-xpQlDovjtlnFa3ENqtkrw130_provenance.
- NP33657.RAmFmJKIXiQsNBnulfXEMF9-xpQlDovjtlnFa3ENqtkrw130_assertion description "[Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP33657.RAmFmJKIXiQsNBnulfXEMF9-xpQlDovjtlnFa3ENqtkrw130_provenance.
- NP33657.RAmFmJKIXiQsNBnulfXEMF9-xpQlDovjtlnFa3ENqtkrw130_assertion evidence source_evidence_curated NP33657.RAmFmJKIXiQsNBnulfXEMF9-xpQlDovjtlnFa3ENqtkrw130_provenance.
- NP33657.RAmFmJKIXiQsNBnulfXEMF9-xpQlDovjtlnFa3ENqtkrw130_assertion SIO_000772 23603762 NP33657.RAmFmJKIXiQsNBnulfXEMF9-xpQlDovjtlnFa3ENqtkrw130_provenance.
- NP33657.RAmFmJKIXiQsNBnulfXEMF9-xpQlDovjtlnFa3ENqtkrw130_assertion wasDerivedFrom ctd_human-20150221 NP33657.RAmFmJKIXiQsNBnulfXEMF9-xpQlDovjtlnFa3ENqtkrw130_provenance.
- NP33657.RAmFmJKIXiQsNBnulfXEMF9-xpQlDovjtlnFa3ENqtkrw130_assertion wasGeneratedBy ECO_0000218 NP33657.RAmFmJKIXiQsNBnulfXEMF9-xpQlDovjtlnFa3ENqtkrw130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP33657.RAmFmJKIXiQsNBnulfXEMF9-xpQlDovjtlnFa3ENqtkrw130_provenance.