Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP921878.RAz9y3ZfNRW2hsEhcopKAAo_DpzEw02oDV0MBF94QveVM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP921878.RAz9y3ZfNRW2hsEhcopKAAo_DpzEw02oDV0MBF94QveVM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP921878.RAz9y3ZfNRW2hsEhcopKAAo_DpzEw02oDV0MBF94QveVM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP921878.RAz9y3ZfNRW2hsEhcopKAAo_DpzEw02oDV0MBF94QveVM130_provenance.
- NP921878.RAz9y3ZfNRW2hsEhcopKAAo_DpzEw02oDV0MBF94QveVM130_assertion description "[Wolman disease (LIPA p.G87V) genotype frequency in people of Iranian-Jewish ancestry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921878.RAz9y3ZfNRW2hsEhcopKAAo_DpzEw02oDV0MBF94QveVM130_provenance.
- NP921878.RAz9y3ZfNRW2hsEhcopKAAo_DpzEw02oDV0MBF94QveVM130_assertion evidence source_evidence_literature NP921878.RAz9y3ZfNRW2hsEhcopKAAo_DpzEw02oDV0MBF94QveVM130_provenance.
- NP921878.RAz9y3ZfNRW2hsEhcopKAAo_DpzEw02oDV0MBF94QveVM130_assertion SIO_000772 21291321 NP921878.RAz9y3ZfNRW2hsEhcopKAAo_DpzEw02oDV0MBF94QveVM130_provenance.
- NP921878.RAz9y3ZfNRW2hsEhcopKAAo_DpzEw02oDV0MBF94QveVM130_assertion wasDerivedFrom befree-20140225 NP921878.RAz9y3ZfNRW2hsEhcopKAAo_DpzEw02oDV0MBF94QveVM130_provenance.
- NP921878.RAz9y3ZfNRW2hsEhcopKAAo_DpzEw02oDV0MBF94QveVM130_assertion wasGeneratedBy ECO_0000203 NP921878.RAz9y3ZfNRW2hsEhcopKAAo_DpzEw02oDV0MBF94QveVM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP921878.RAz9y3ZfNRW2hsEhcopKAAo_DpzEw02oDV0MBF94QveVM130_provenance.