Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP935282.RAjau2OjPcMTwHlVPDOchydd5DG9s_kTTO1tIcQB3f4VE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP935282.RAjau2OjPcMTwHlVPDOchydd5DG9s_kTTO1tIcQB3f4VE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP935282.RAjau2OjPcMTwHlVPDOchydd5DG9s_kTTO1tIcQB3f4VE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP935282.RAjau2OjPcMTwHlVPDOchydd5DG9s_kTTO1tIcQB3f4VE130_provenance.
- NP935282.RAjau2OjPcMTwHlVPDOchydd5DG9s_kTTO1tIcQB3f4VE130_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." NP935282.RAjau2OjPcMTwHlVPDOchydd5DG9s_kTTO1tIcQB3f4VE130_provenance.
- NP935282.RAjau2OjPcMTwHlVPDOchydd5DG9s_kTTO1tIcQB3f4VE130_assertion evidence source_evidence_literature NP935282.RAjau2OjPcMTwHlVPDOchydd5DG9s_kTTO1tIcQB3f4VE130_provenance.
- NP935282.RAjau2OjPcMTwHlVPDOchydd5DG9s_kTTO1tIcQB3f4VE130_assertion SIO_000772 16650080 NP935282.RAjau2OjPcMTwHlVPDOchydd5DG9s_kTTO1tIcQB3f4VE130_provenance.
- NP935282.RAjau2OjPcMTwHlVPDOchydd5DG9s_kTTO1tIcQB3f4VE130_assertion wasDerivedFrom befree-20140225 NP935282.RAjau2OjPcMTwHlVPDOchydd5DG9s_kTTO1tIcQB3f4VE130_provenance.
- NP935282.RAjau2OjPcMTwHlVPDOchydd5DG9s_kTTO1tIcQB3f4VE130_assertion wasGeneratedBy ECO_0000203 NP935282.RAjau2OjPcMTwHlVPDOchydd5DG9s_kTTO1tIcQB3f4VE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP935282.RAjau2OjPcMTwHlVPDOchydd5DG9s_kTTO1tIcQB3f4VE130_provenance.