Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP859270.RAbesD5vC1_CJYEryOx0c2_hWA3sbEn_qrAx3AJTBCq1o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP859270.RAbesD5vC1_CJYEryOx0c2_hWA3sbEn_qrAx3AJTBCq1o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP859270.RAbesD5vC1_CJYEryOx0c2_hWA3sbEn_qrAx3AJTBCq1o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP859270.RAbesD5vC1_CJYEryOx0c2_hWA3sbEn_qrAx3AJTBCq1o130_provenance.
- NP859270.RAbesD5vC1_CJYEryOx0c2_hWA3sbEn_qrAx3AJTBCq1o130_assertion wasGeneratedBy ECO_0000203 NP859270.RAbesD5vC1_CJYEryOx0c2_hWA3sbEn_qrAx3AJTBCq1o130_provenance.
- NP859270.RAbesD5vC1_CJYEryOx0c2_hWA3sbEn_qrAx3AJTBCq1o130_assertion wasDerivedFrom befree-20140225 NP859270.RAbesD5vC1_CJYEryOx0c2_hWA3sbEn_qrAx3AJTBCq1o130_provenance.
- NP859270.RAbesD5vC1_CJYEryOx0c2_hWA3sbEn_qrAx3AJTBCq1o130_assertion SIO_000772 15466077 NP859270.RAbesD5vC1_CJYEryOx0c2_hWA3sbEn_qrAx3AJTBCq1o130_provenance.
- NP859270.RAbesD5vC1_CJYEryOx0c2_hWA3sbEn_qrAx3AJTBCq1o130_assertion evidence source_evidence_literature NP859270.RAbesD5vC1_CJYEryOx0c2_hWA3sbEn_qrAx3AJTBCq1o130_provenance.
- NP859270.RAbesD5vC1_CJYEryOx0c2_hWA3sbEn_qrAx3AJTBCq1o130_assertion description "[It is necessary to distinguish between lethal mutations leading to diseases such as MCAD and LQTS, and polymorphisms (for instance, in the IL-10 gene and mtDNA) that are normal gene variants but might be suboptimal in critical situations and thus predispose infants to sudden infant death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP859270.RAbesD5vC1_CJYEryOx0c2_hWA3sbEn_qrAx3AJTBCq1o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP859270.RAbesD5vC1_CJYEryOx0c2_hWA3sbEn_qrAx3AJTBCq1o130_provenance.