Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP234900.RAHHjZY2WNt8jZy7CGi0e7vP-KfRcxc0BoeIz_D-EV1zA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP234900.RAHHjZY2WNt8jZy7CGi0e7vP-KfRcxc0BoeIz_D-EV1zA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP234900.RAHHjZY2WNt8jZy7CGi0e7vP-KfRcxc0BoeIz_D-EV1zA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP234900.RAHHjZY2WNt8jZy7CGi0e7vP-KfRcxc0BoeIz_D-EV1zA130_provenance.
- NP234900.RAHHjZY2WNt8jZy7CGi0e7vP-KfRcxc0BoeIz_D-EV1zA130_assertion description "[In humans, mutations in the FALDH gene cause Sj�gren-Larsson syndrome (SLS), which is characterized by ichthyosis, mental retardation and spasticity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP234900.RAHHjZY2WNt8jZy7CGi0e7vP-KfRcxc0BoeIz_D-EV1zA130_provenance.
- NP234900.RAHHjZY2WNt8jZy7CGi0e7vP-KfRcxc0BoeIz_D-EV1zA130_assertion evidence source_evidence_literature NP234900.RAHHjZY2WNt8jZy7CGi0e7vP-KfRcxc0BoeIz_D-EV1zA130_provenance.
- NP234900.RAHHjZY2WNt8jZy7CGi0e7vP-KfRcxc0BoeIz_D-EV1zA130_assertion SIO_000772 11306053 NP234900.RAHHjZY2WNt8jZy7CGi0e7vP-KfRcxc0BoeIz_D-EV1zA130_provenance.
- NP234900.RAHHjZY2WNt8jZy7CGi0e7vP-KfRcxc0BoeIz_D-EV1zA130_assertion wasDerivedFrom befree-20150227 NP234900.RAHHjZY2WNt8jZy7CGi0e7vP-KfRcxc0BoeIz_D-EV1zA130_provenance.
- NP234900.RAHHjZY2WNt8jZy7CGi0e7vP-KfRcxc0BoeIz_D-EV1zA130_assertion wasGeneratedBy ECO_0000203 NP234900.RAHHjZY2WNt8jZy7CGi0e7vP-KfRcxc0BoeIz_D-EV1zA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP234900.RAHHjZY2WNt8jZy7CGi0e7vP-KfRcxc0BoeIz_D-EV1zA130_provenance.