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- source_evidence_literature type ECO_0000212 NP708208.RA9Fibtm9Wj_02cQWohG2HGV7cQc3pWb_ncje-m8mrc7I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP708208.RA9Fibtm9Wj_02cQWohG2HGV7cQc3pWb_ncje-m8mrc7I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP708208.RA9Fibtm9Wj_02cQWohG2HGV7cQc3pWb_ncje-m8mrc7I130_provenance.
- NP708208.RA9Fibtm9Wj_02cQWohG2HGV7cQc3pWb_ncje-m8mrc7I130_assertion description "[Mutations in the fatty acid 2-hydroxylase gene are associated with leukodystrophy with spastic paraparesis and dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708208.RA9Fibtm9Wj_02cQWohG2HGV7cQc3pWb_ncje-m8mrc7I130_provenance.
- NP708208.RA9Fibtm9Wj_02cQWohG2HGV7cQc3pWb_ncje-m8mrc7I130_assertion evidence source_evidence_literature NP708208.RA9Fibtm9Wj_02cQWohG2HGV7cQc3pWb_ncje-m8mrc7I130_provenance.
- NP708208.RA9Fibtm9Wj_02cQWohG2HGV7cQc3pWb_ncje-m8mrc7I130_assertion SIO_000772 19068277 NP708208.RA9Fibtm9Wj_02cQWohG2HGV7cQc3pWb_ncje-m8mrc7I130_provenance.
- NP708208.RA9Fibtm9Wj_02cQWohG2HGV7cQc3pWb_ncje-m8mrc7I130_assertion wasDerivedFrom befree-2016 NP708208.RA9Fibtm9Wj_02cQWohG2HGV7cQc3pWb_ncje-m8mrc7I130_provenance.
- NP708208.RA9Fibtm9Wj_02cQWohG2HGV7cQc3pWb_ncje-m8mrc7I130_assertion wasGeneratedBy ECO_0000203 NP708208.RA9Fibtm9Wj_02cQWohG2HGV7cQc3pWb_ncje-m8mrc7I130_provenance.
- befree-2016 importedOn "2016-02-19" NP708208.RA9Fibtm9Wj_02cQWohG2HGV7cQc3pWb_ncje-m8mrc7I130_provenance.