Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP32872.RA69H24qrTm8CLV-iO_4lHbaVFJmEAN3vnxkv9WLeELK4130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP32872.RA69H24qrTm8CLV-iO_4lHbaVFJmEAN3vnxkv9WLeELK4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP32872.RA69H24qrTm8CLV-iO_4lHbaVFJmEAN3vnxkv9WLeELK4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP32872.RA69H24qrTm8CLV-iO_4lHbaVFJmEAN3vnxkv9WLeELK4130_provenance.
- NP32872.RA69H24qrTm8CLV-iO_4lHbaVFJmEAN3vnxkv9WLeELK4130_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." NP32872.RA69H24qrTm8CLV-iO_4lHbaVFJmEAN3vnxkv9WLeELK4130_provenance.
- NP32872.RA69H24qrTm8CLV-iO_4lHbaVFJmEAN3vnxkv9WLeELK4130_assertion evidence source_evidence_curated NP32872.RA69H24qrTm8CLV-iO_4lHbaVFJmEAN3vnxkv9WLeELK4130_provenance.
- NP32872.RA69H24qrTm8CLV-iO_4lHbaVFJmEAN3vnxkv9WLeELK4130_assertion SIO_000772 23603762 NP32872.RA69H24qrTm8CLV-iO_4lHbaVFJmEAN3vnxkv9WLeELK4130_provenance.
- NP32872.RA69H24qrTm8CLV-iO_4lHbaVFJmEAN3vnxkv9WLeELK4130_assertion wasDerivedFrom ctd_human-2016 NP32872.RA69H24qrTm8CLV-iO_4lHbaVFJmEAN3vnxkv9WLeELK4130_provenance.
- NP32872.RA69H24qrTm8CLV-iO_4lHbaVFJmEAN3vnxkv9WLeELK4130_assertion wasGeneratedBy ECO_0000218 NP32872.RA69H24qrTm8CLV-iO_4lHbaVFJmEAN3vnxkv9WLeELK4130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP32872.RA69H24qrTm8CLV-iO_4lHbaVFJmEAN3vnxkv9WLeELK4130_provenance.