Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP20945.RANX5iBGMEiqQbLAiClRWx3VnC1pz4efJGftNvBdlKiUc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP20945.RANX5iBGMEiqQbLAiClRWx3VnC1pz4efJGftNvBdlKiUc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP20945.RANX5iBGMEiqQbLAiClRWx3VnC1pz4efJGftNvBdlKiUc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP20945.RANX5iBGMEiqQbLAiClRWx3VnC1pz4efJGftNvBdlKiUc130_provenance.
- NP20945.RANX5iBGMEiqQbLAiClRWx3VnC1pz4efJGftNvBdlKiUc130_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." NP20945.RANX5iBGMEiqQbLAiClRWx3VnC1pz4efJGftNvBdlKiUc130_provenance.
- NP20945.RANX5iBGMEiqQbLAiClRWx3VnC1pz4efJGftNvBdlKiUc130_assertion evidence source_evidence_curated NP20945.RANX5iBGMEiqQbLAiClRWx3VnC1pz4efJGftNvBdlKiUc130_provenance.
- NP20945.RANX5iBGMEiqQbLAiClRWx3VnC1pz4efJGftNvBdlKiUc130_assertion SIO_000772 23603762 NP20945.RANX5iBGMEiqQbLAiClRWx3VnC1pz4efJGftNvBdlKiUc130_provenance.
- NP20945.RANX5iBGMEiqQbLAiClRWx3VnC1pz4efJGftNvBdlKiUc130_assertion wasDerivedFrom ctd_human-20130708 NP20945.RANX5iBGMEiqQbLAiClRWx3VnC1pz4efJGftNvBdlKiUc130_provenance.
- NP20945.RANX5iBGMEiqQbLAiClRWx3VnC1pz4efJGftNvBdlKiUc130_assertion wasGeneratedBy ECO_0000218 NP20945.RANX5iBGMEiqQbLAiClRWx3VnC1pz4efJGftNvBdlKiUc130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP20945.RANX5iBGMEiqQbLAiClRWx3VnC1pz4efJGftNvBdlKiUc130_provenance.