Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP337645.RABkFJxxYv2BKYrtS3Jgj4kp3g8DoTXChw07J1UjXuBis130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP337645.RABkFJxxYv2BKYrtS3Jgj4kp3g8DoTXChw07J1UjXuBis130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP337645.RABkFJxxYv2BKYrtS3Jgj4kp3g8DoTXChw07J1UjXuBis130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP337645.RABkFJxxYv2BKYrtS3Jgj4kp3g8DoTXChw07J1UjXuBis130_provenance.
- NP337645.RABkFJxxYv2BKYrtS3Jgj4kp3g8DoTXChw07J1UjXuBis130_assertion description "[Wolman disease (WD) is a rare inherited condition caused by lysosomal acid lipase (LAL) deficiency first described in Iranian-Jewish (IJ) children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP337645.RABkFJxxYv2BKYrtS3Jgj4kp3g8DoTXChw07J1UjXuBis130_provenance.
- NP337645.RABkFJxxYv2BKYrtS3Jgj4kp3g8DoTXChw07J1UjXuBis130_assertion evidence source_evidence_literature NP337645.RABkFJxxYv2BKYrtS3Jgj4kp3g8DoTXChw07J1UjXuBis130_provenance.
- NP337645.RABkFJxxYv2BKYrtS3Jgj4kp3g8DoTXChw07J1UjXuBis130_assertion SIO_000772 21291321 NP337645.RABkFJxxYv2BKYrtS3Jgj4kp3g8DoTXChw07J1UjXuBis130_provenance.
- NP337645.RABkFJxxYv2BKYrtS3Jgj4kp3g8DoTXChw07J1UjXuBis130_assertion wasDerivedFrom befree-20140225 NP337645.RABkFJxxYv2BKYrtS3Jgj4kp3g8DoTXChw07J1UjXuBis130_provenance.
- NP337645.RABkFJxxYv2BKYrtS3Jgj4kp3g8DoTXChw07J1UjXuBis130_assertion wasGeneratedBy ECO_0000203 NP337645.RABkFJxxYv2BKYrtS3Jgj4kp3g8DoTXChw07J1UjXuBis130_provenance.
- befree-20140225 importedOn "2014-02-25" NP337645.RABkFJxxYv2BKYrtS3Jgj4kp3g8DoTXChw07J1UjXuBis130_provenance.