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- source_evidence_literature type ECO_0000212 NP690083.RA_3BGC13uKUcmX94mqJC0OOzM3CKbbJlartsp_9iqIAE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690083.RA_3BGC13uKUcmX94mqJC0OOzM3CKbbJlartsp_9iqIAE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690083.RA_3BGC13uKUcmX94mqJC0OOzM3CKbbJlartsp_9iqIAE130_provenance.
- NP690083.RA_3BGC13uKUcmX94mqJC0OOzM3CKbbJlartsp_9iqIAE130_assertion description "[Autosomal recessive form of hypophosphatemic rickets was mapped to chromosome 4q21 and identified homozygous mutations in dentin matrix protein 1 (DMP1) gene, which encodes a non-collagenous bone matrix protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690083.RA_3BGC13uKUcmX94mqJC0OOzM3CKbbJlartsp_9iqIAE130_provenance.
- NP690083.RA_3BGC13uKUcmX94mqJC0OOzM3CKbbJlartsp_9iqIAE130_assertion evidence source_evidence_literature NP690083.RA_3BGC13uKUcmX94mqJC0OOzM3CKbbJlartsp_9iqIAE130_provenance.
- NP690083.RA_3BGC13uKUcmX94mqJC0OOzM3CKbbJlartsp_9iqIAE130_assertion SIO_000772 17635744 NP690083.RA_3BGC13uKUcmX94mqJC0OOzM3CKbbJlartsp_9iqIAE130_provenance.
- NP690083.RA_3BGC13uKUcmX94mqJC0OOzM3CKbbJlartsp_9iqIAE130_assertion wasDerivedFrom befree-20140225 NP690083.RA_3BGC13uKUcmX94mqJC0OOzM3CKbbJlartsp_9iqIAE130_provenance.
- NP690083.RA_3BGC13uKUcmX94mqJC0OOzM3CKbbJlartsp_9iqIAE130_assertion wasGeneratedBy ECO_0000203 NP690083.RA_3BGC13uKUcmX94mqJC0OOzM3CKbbJlartsp_9iqIAE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP690083.RA_3BGC13uKUcmX94mqJC0OOzM3CKbbJlartsp_9iqIAE130_provenance.