Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP927589.RAUCqhIc7PLLDQDFmZglnii67ZI65UJrVh4urvLSWAcfE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP927589.RAUCqhIc7PLLDQDFmZglnii67ZI65UJrVh4urvLSWAcfE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP927589.RAUCqhIc7PLLDQDFmZglnii67ZI65UJrVh4urvLSWAcfE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP927589.RAUCqhIc7PLLDQDFmZglnii67ZI65UJrVh4urvLSWAcfE130_provenance.
- NP927589.RAUCqhIc7PLLDQDFmZglnii67ZI65UJrVh4urvLSWAcfE130_assertion description "[In a nationwide study conducted in Japan between 1999 and 2009, the authors identified 51 different L1CAM gene mutations in 56 families with XLH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927589.RAUCqhIc7PLLDQDFmZglnii67ZI65UJrVh4urvLSWAcfE130_provenance.
- NP927589.RAUCqhIc7PLLDQDFmZglnii67ZI65UJrVh4urvLSWAcfE130_assertion evidence source_evidence_literature NP927589.RAUCqhIc7PLLDQDFmZglnii67ZI65UJrVh4urvLSWAcfE130_provenance.
- NP927589.RAUCqhIc7PLLDQDFmZglnii67ZI65UJrVh4urvLSWAcfE130_assertion SIO_000772 21961551 NP927589.RAUCqhIc7PLLDQDFmZglnii67ZI65UJrVh4urvLSWAcfE130_provenance.
- NP927589.RAUCqhIc7PLLDQDFmZglnii67ZI65UJrVh4urvLSWAcfE130_assertion wasDerivedFrom befree-2016 NP927589.RAUCqhIc7PLLDQDFmZglnii67ZI65UJrVh4urvLSWAcfE130_provenance.
- NP927589.RAUCqhIc7PLLDQDFmZglnii67ZI65UJrVh4urvLSWAcfE130_assertion wasGeneratedBy ECO_0000203 NP927589.RAUCqhIc7PLLDQDFmZglnii67ZI65UJrVh4urvLSWAcfE130_provenance.
- befree-2016 importedOn "2016-02-19" NP927589.RAUCqhIc7PLLDQDFmZglnii67ZI65UJrVh4urvLSWAcfE130_provenance.