Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP529958.RAhyFz0NPe9D80815WQf2pZIR1WRLRD06rgmj6DfZ6Kms130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP529958.RAhyFz0NPe9D80815WQf2pZIR1WRLRD06rgmj6DfZ6Kms130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP529958.RAhyFz0NPe9D80815WQf2pZIR1WRLRD06rgmj6DfZ6Kms130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP529958.RAhyFz0NPe9D80815WQf2pZIR1WRLRD06rgmj6DfZ6Kms130_provenance.
- NP529958.RAhyFz0NPe9D80815WQf2pZIR1WRLRD06rgmj6DfZ6Kms130_assertion description "[The L1CAM gene, which is located in Xq28 and codes for a neuronal cell adhesion molecule, is involved in three distinct conditions: HSAS (hydrocephalus-stenosis of the aqueduct of Sylvius), MASA (mental retardation, aphasia, shuffling gait, adductus thumbs), and SPG1 (spastic paraplegia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP529958.RAhyFz0NPe9D80815WQf2pZIR1WRLRD06rgmj6DfZ6Kms130_provenance.
- NP529958.RAhyFz0NPe9D80815WQf2pZIR1WRLRD06rgmj6DfZ6Kms130_assertion evidence source_evidence_literature NP529958.RAhyFz0NPe9D80815WQf2pZIR1WRLRD06rgmj6DfZ6Kms130_provenance.
- NP529958.RAhyFz0NPe9D80815WQf2pZIR1WRLRD06rgmj6DfZ6Kms130_assertion SIO_000772 9744477 NP529958.RAhyFz0NPe9D80815WQf2pZIR1WRLRD06rgmj6DfZ6Kms130_provenance.
- NP529958.RAhyFz0NPe9D80815WQf2pZIR1WRLRD06rgmj6DfZ6Kms130_assertion wasDerivedFrom befree-20150227 NP529958.RAhyFz0NPe9D80815WQf2pZIR1WRLRD06rgmj6DfZ6Kms130_provenance.
- NP529958.RAhyFz0NPe9D80815WQf2pZIR1WRLRD06rgmj6DfZ6Kms130_assertion wasGeneratedBy ECO_0000203 NP529958.RAhyFz0NPe9D80815WQf2pZIR1WRLRD06rgmj6DfZ6Kms130_provenance.
- befree-20150227 importedOn "2015-02-27" NP529958.RAhyFz0NPe9D80815WQf2pZIR1WRLRD06rgmj6DfZ6Kms130_provenance.