Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP491851.RAlQolzUjQV9pny0EHZUJ_PKz1u1cq2tw-XQrd-uRTxCU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP491851.RAlQolzUjQV9pny0EHZUJ_PKz1u1cq2tw-XQrd-uRTxCU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP491851.RAlQolzUjQV9pny0EHZUJ_PKz1u1cq2tw-XQrd-uRTxCU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP491851.RAlQolzUjQV9pny0EHZUJ_PKz1u1cq2tw-XQrd-uRTxCU130_provenance.
- NP491851.RAlQolzUjQV9pny0EHZUJ_PKz1u1cq2tw-XQrd-uRTxCU130_assertion description "[No association was found between polymorphisms of IL1B C(-31)T/IL1RN VNTR or their haplotypes and CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP491851.RAlQolzUjQV9pny0EHZUJ_PKz1u1cq2tw-XQrd-uRTxCU130_provenance.
- NP491851.RAlQolzUjQV9pny0EHZUJ_PKz1u1cq2tw-XQrd-uRTxCU130_assertion evidence source_evidence_literature NP491851.RAlQolzUjQV9pny0EHZUJ_PKz1u1cq2tw-XQrd-uRTxCU130_provenance.
- NP491851.RAlQolzUjQV9pny0EHZUJ_PKz1u1cq2tw-XQrd-uRTxCU130_assertion SIO_000772 21840356 NP491851.RAlQolzUjQV9pny0EHZUJ_PKz1u1cq2tw-XQrd-uRTxCU130_provenance.
- NP491851.RAlQolzUjQV9pny0EHZUJ_PKz1u1cq2tw-XQrd-uRTxCU130_assertion wasDerivedFrom befree-20150227 NP491851.RAlQolzUjQV9pny0EHZUJ_PKz1u1cq2tw-XQrd-uRTxCU130_provenance.
- NP491851.RAlQolzUjQV9pny0EHZUJ_PKz1u1cq2tw-XQrd-uRTxCU130_assertion wasGeneratedBy ECO_0000203 NP491851.RAlQolzUjQV9pny0EHZUJ_PKz1u1cq2tw-XQrd-uRTxCU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP491851.RAlQolzUjQV9pny0EHZUJ_PKz1u1cq2tw-XQrd-uRTxCU130_provenance.