Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP718571.RAuG3L_nVVBLUDp_uQsC9s5BQ8MoyUw1KqmI-qrD44pIU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718571.RAuG3L_nVVBLUDp_uQsC9s5BQ8MoyUw1KqmI-qrD44pIU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718571.RAuG3L_nVVBLUDp_uQsC9s5BQ8MoyUw1KqmI-qrD44pIU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718571.RAuG3L_nVVBLUDp_uQsC9s5BQ8MoyUw1KqmI-qrD44pIU130_provenance.
- NP718571.RAuG3L_nVVBLUDp_uQsC9s5BQ8MoyUw1KqmI-qrD44pIU130_assertion description "[Recessive mutations in ELOVL4 cause ichthyosis, intellectual disability, and spastic quadriplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718571.RAuG3L_nVVBLUDp_uQsC9s5BQ8MoyUw1KqmI-qrD44pIU130_provenance.
- NP718571.RAuG3L_nVVBLUDp_uQsC9s5BQ8MoyUw1KqmI-qrD44pIU130_assertion evidence source_evidence_literature NP718571.RAuG3L_nVVBLUDp_uQsC9s5BQ8MoyUw1KqmI-qrD44pIU130_provenance.
- NP718571.RAuG3L_nVVBLUDp_uQsC9s5BQ8MoyUw1KqmI-qrD44pIU130_assertion SIO_000772 22100072 NP718571.RAuG3L_nVVBLUDp_uQsC9s5BQ8MoyUw1KqmI-qrD44pIU130_provenance.
- NP718571.RAuG3L_nVVBLUDp_uQsC9s5BQ8MoyUw1KqmI-qrD44pIU130_assertion wasDerivedFrom befree-20150227 NP718571.RAuG3L_nVVBLUDp_uQsC9s5BQ8MoyUw1KqmI-qrD44pIU130_provenance.
- NP718571.RAuG3L_nVVBLUDp_uQsC9s5BQ8MoyUw1KqmI-qrD44pIU130_assertion wasGeneratedBy ECO_0000203 NP718571.RAuG3L_nVVBLUDp_uQsC9s5BQ8MoyUw1KqmI-qrD44pIU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP718571.RAuG3L_nVVBLUDp_uQsC9s5BQ8MoyUw1KqmI-qrD44pIU130_provenance.