Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP768418.RAuscuHDUDFdTfn-XbU43RdSYfhbWPGDV62_pBPSbj5eE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP768418.RAuscuHDUDFdTfn-XbU43RdSYfhbWPGDV62_pBPSbj5eE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768418.RAuscuHDUDFdTfn-XbU43RdSYfhbWPGDV62_pBPSbj5eE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768418.RAuscuHDUDFdTfn-XbU43RdSYfhbWPGDV62_pBPSbj5eE130_provenance.
- NP768418.RAuscuHDUDFdTfn-XbU43RdSYfhbWPGDV62_pBPSbj5eE130_assertion description "[Mutations in the L1CAM gene cause neurological abnormalities of variable severity, including congenital hydrocephalus, agenesis of the corpus callosum, spastic paraplegia, bilaterally adducted thumbs, aphasia, and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768418.RAuscuHDUDFdTfn-XbU43RdSYfhbWPGDV62_pBPSbj5eE130_provenance.
- NP768418.RAuscuHDUDFdTfn-XbU43RdSYfhbWPGDV62_pBPSbj5eE130_assertion evidence source_evidence_literature NP768418.RAuscuHDUDFdTfn-XbU43RdSYfhbWPGDV62_pBPSbj5eE130_provenance.
- NP768418.RAuscuHDUDFdTfn-XbU43RdSYfhbWPGDV62_pBPSbj5eE130_assertion SIO_000772 16650080 NP768418.RAuscuHDUDFdTfn-XbU43RdSYfhbWPGDV62_pBPSbj5eE130_provenance.
- NP768418.RAuscuHDUDFdTfn-XbU43RdSYfhbWPGDV62_pBPSbj5eE130_assertion wasDerivedFrom befree-20150227 NP768418.RAuscuHDUDFdTfn-XbU43RdSYfhbWPGDV62_pBPSbj5eE130_provenance.
- NP768418.RAuscuHDUDFdTfn-XbU43RdSYfhbWPGDV62_pBPSbj5eE130_assertion wasGeneratedBy ECO_0000203 NP768418.RAuscuHDUDFdTfn-XbU43RdSYfhbWPGDV62_pBPSbj5eE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP768418.RAuscuHDUDFdTfn-XbU43RdSYfhbWPGDV62_pBPSbj5eE130_provenance.