Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP224565.RA8E7pu4wl9PwW9xKMpQ0FdSA_b4ibyk_TLZX7AmWsThs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP224565.RA8E7pu4wl9PwW9xKMpQ0FdSA_b4ibyk_TLZX7AmWsThs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP224565.RA8E7pu4wl9PwW9xKMpQ0FdSA_b4ibyk_TLZX7AmWsThs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP224565.RA8E7pu4wl9PwW9xKMpQ0FdSA_b4ibyk_TLZX7AmWsThs130_provenance.
- NP224565.RA8E7pu4wl9PwW9xKMpQ0FdSA_b4ibyk_TLZX7AmWsThs130_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." NP224565.RA8E7pu4wl9PwW9xKMpQ0FdSA_b4ibyk_TLZX7AmWsThs130_provenance.
- NP224565.RA8E7pu4wl9PwW9xKMpQ0FdSA_b4ibyk_TLZX7AmWsThs130_assertion evidence source_evidence_literature NP224565.RA8E7pu4wl9PwW9xKMpQ0FdSA_b4ibyk_TLZX7AmWsThs130_provenance.
- NP224565.RA8E7pu4wl9PwW9xKMpQ0FdSA_b4ibyk_TLZX7AmWsThs130_assertion SIO_000772 16650080 NP224565.RA8E7pu4wl9PwW9xKMpQ0FdSA_b4ibyk_TLZX7AmWsThs130_provenance.
- NP224565.RA8E7pu4wl9PwW9xKMpQ0FdSA_b4ibyk_TLZX7AmWsThs130_assertion wasDerivedFrom befree-20140225 NP224565.RA8E7pu4wl9PwW9xKMpQ0FdSA_b4ibyk_TLZX7AmWsThs130_provenance.
- NP224565.RA8E7pu4wl9PwW9xKMpQ0FdSA_b4ibyk_TLZX7AmWsThs130_assertion wasGeneratedBy ECO_0000203 NP224565.RA8E7pu4wl9PwW9xKMpQ0FdSA_b4ibyk_TLZX7AmWsThs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP224565.RA8E7pu4wl9PwW9xKMpQ0FdSA_b4ibyk_TLZX7AmWsThs130_provenance.