Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP768228.RAk4stfP0XAmTjVsop1bxaVOybCOCDIJG3B71zh9PsEHA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP768228.RAk4stfP0XAmTjVsop1bxaVOybCOCDIJG3B71zh9PsEHA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768228.RAk4stfP0XAmTjVsop1bxaVOybCOCDIJG3B71zh9PsEHA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768228.RAk4stfP0XAmTjVsop1bxaVOybCOCDIJG3B71zh9PsEHA130_provenance.
- NP768228.RAk4stfP0XAmTjVsop1bxaVOybCOCDIJG3B71zh9PsEHA130_assertion description "[The abnormal development of axon tracts resulting in the corpus callosum hypoplasia and adducted thumbs appears to be caused by malfunction of the cytoplasmic domain of L1CAM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768228.RAk4stfP0XAmTjVsop1bxaVOybCOCDIJG3B71zh9PsEHA130_provenance.
- NP768228.RAk4stfP0XAmTjVsop1bxaVOybCOCDIJG3B71zh9PsEHA130_assertion evidence source_evidence_literature NP768228.RAk4stfP0XAmTjVsop1bxaVOybCOCDIJG3B71zh9PsEHA130_provenance.
- NP768228.RAk4stfP0XAmTjVsop1bxaVOybCOCDIJG3B71zh9PsEHA130_assertion SIO_000772 15904436 NP768228.RAk4stfP0XAmTjVsop1bxaVOybCOCDIJG3B71zh9PsEHA130_provenance.
- NP768228.RAk4stfP0XAmTjVsop1bxaVOybCOCDIJG3B71zh9PsEHA130_assertion wasDerivedFrom befree-20150227 NP768228.RAk4stfP0XAmTjVsop1bxaVOybCOCDIJG3B71zh9PsEHA130_provenance.
- NP768228.RAk4stfP0XAmTjVsop1bxaVOybCOCDIJG3B71zh9PsEHA130_assertion wasGeneratedBy ECO_0000203 NP768228.RAk4stfP0XAmTjVsop1bxaVOybCOCDIJG3B71zh9PsEHA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP768228.RAk4stfP0XAmTjVsop1bxaVOybCOCDIJG3B71zh9PsEHA130_provenance.