Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP96411.RAJGcVLTUJONdS-3qsEHmTiiCiUZw1oqa7a9SSeGymgN4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP96411.RAJGcVLTUJONdS-3qsEHmTiiCiUZw1oqa7a9SSeGymgN4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP96411.RAJGcVLTUJONdS-3qsEHmTiiCiUZw1oqa7a9SSeGymgN4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP96411.RAJGcVLTUJONdS-3qsEHmTiiCiUZw1oqa7a9SSeGymgN4130_provenance.
- NP96411.RAJGcVLTUJONdS-3qsEHmTiiCiUZw1oqa7a9SSeGymgN4130_assertion description "[We have identified nine genetic variants associated with fasting proinsulin. Our findings illuminate the biology underlying glucose homeostasis and T2D development in humans and argue against a direct role of proinsulin in coronary artery disease pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96411.RAJGcVLTUJONdS-3qsEHmTiiCiUZw1oqa7a9SSeGymgN4130_provenance.
- NP96411.RAJGcVLTUJONdS-3qsEHmTiiCiUZw1oqa7a9SSeGymgN4130_assertion evidence source_evidence_literature NP96411.RAJGcVLTUJONdS-3qsEHmTiiCiUZw1oqa7a9SSeGymgN4130_provenance.
- NP96411.RAJGcVLTUJONdS-3qsEHmTiiCiUZw1oqa7a9SSeGymgN4130_assertion SIO_000772 21873549 NP96411.RAJGcVLTUJONdS-3qsEHmTiiCiUZw1oqa7a9SSeGymgN4130_provenance.
- NP96411.RAJGcVLTUJONdS-3qsEHmTiiCiUZw1oqa7a9SSeGymgN4130_assertion wasDerivedFrom gad-20130706 NP96411.RAJGcVLTUJONdS-3qsEHmTiiCiUZw1oqa7a9SSeGymgN4130_provenance.
- NP96411.RAJGcVLTUJONdS-3qsEHmTiiCiUZw1oqa7a9SSeGymgN4130_assertion wasGeneratedBy ECO_0000203 NP96411.RAJGcVLTUJONdS-3qsEHmTiiCiUZw1oqa7a9SSeGymgN4130_provenance.
- gad-20130706 importedOn "2013-07-06" NP96411.RAJGcVLTUJONdS-3qsEHmTiiCiUZw1oqa7a9SSeGymgN4130_provenance.