Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP738821.RADPvEhoLYGZdKLJT-tMJfcBjHhdIKNJr5M6IOXS9_YZo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP738821.RADPvEhoLYGZdKLJT-tMJfcBjHhdIKNJr5M6IOXS9_YZo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP738821.RADPvEhoLYGZdKLJT-tMJfcBjHhdIKNJr5M6IOXS9_YZo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP738821.RADPvEhoLYGZdKLJT-tMJfcBjHhdIKNJr5M6IOXS9_YZo130_provenance.
- NP738821.RADPvEhoLYGZdKLJT-tMJfcBjHhdIKNJr5M6IOXS9_YZo130_assertion description "[In this study, we evaluated 17 single nucleotide polymorphisms (SNPs) across 37 kb of C1QA, C1QB and C1QC in a lupus cohort of individuals of the African-American and Hispanic origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP738821.RADPvEhoLYGZdKLJT-tMJfcBjHhdIKNJr5M6IOXS9_YZo130_provenance.
- NP738821.RADPvEhoLYGZdKLJT-tMJfcBjHhdIKNJr5M6IOXS9_YZo130_assertion evidence source_evidence_literature NP738821.RADPvEhoLYGZdKLJT-tMJfcBjHhdIKNJr5M6IOXS9_YZo130_provenance.
- NP738821.RADPvEhoLYGZdKLJT-tMJfcBjHhdIKNJr5M6IOXS9_YZo130_assertion SIO_000772 19440201 NP738821.RADPvEhoLYGZdKLJT-tMJfcBjHhdIKNJr5M6IOXS9_YZo130_provenance.
- NP738821.RADPvEhoLYGZdKLJT-tMJfcBjHhdIKNJr5M6IOXS9_YZo130_assertion wasDerivedFrom befree-2016 NP738821.RADPvEhoLYGZdKLJT-tMJfcBjHhdIKNJr5M6IOXS9_YZo130_provenance.
- NP738821.RADPvEhoLYGZdKLJT-tMJfcBjHhdIKNJr5M6IOXS9_YZo130_assertion wasGeneratedBy ECO_0000203 NP738821.RADPvEhoLYGZdKLJT-tMJfcBjHhdIKNJr5M6IOXS9_YZo130_provenance.
- befree-2016 importedOn "2016-02-19" NP738821.RADPvEhoLYGZdKLJT-tMJfcBjHhdIKNJr5M6IOXS9_YZo130_provenance.