Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP90855.RAjjh1HtE2YHNE7rm804K6GeNJICLCjVTnXZ5rjyC5QOA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP90855.RAjjh1HtE2YHNE7rm804K6GeNJICLCjVTnXZ5rjyC5QOA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP90855.RAjjh1HtE2YHNE7rm804K6GeNJICLCjVTnXZ5rjyC5QOA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP90855.RAjjh1HtE2YHNE7rm804K6GeNJICLCjVTnXZ5rjyC5QOA130_provenance.
- NP90855.RAjjh1HtE2YHNE7rm804K6GeNJICLCjVTnXZ5rjyC5QOA130_assertion description "[This study is of great importance (i) particularly in the context of the diversity caused by the population migrations, we may observe today in our hospitals (ii) to confirm that the Pygmy population with distinctive frequencies (absence of the HPA-1b, HP]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP90855.RAjjh1HtE2YHNE7rm804K6GeNJICLCjVTnXZ5rjyC5QOA130_provenance.
- NP90855.RAjjh1HtE2YHNE7rm804K6GeNJICLCjVTnXZ5rjyC5QOA130_assertion evidence source_evidence_literature NP90855.RAjjh1HtE2YHNE7rm804K6GeNJICLCjVTnXZ5rjyC5QOA130_provenance.
- NP90855.RAjjh1HtE2YHNE7rm804K6GeNJICLCjVTnXZ5rjyC5QOA130_assertion SIO_000772 15730528 NP90855.RAjjh1HtE2YHNE7rm804K6GeNJICLCjVTnXZ5rjyC5QOA130_provenance.
- NP90855.RAjjh1HtE2YHNE7rm804K6GeNJICLCjVTnXZ5rjyC5QOA130_assertion wasDerivedFrom gad-20150221 NP90855.RAjjh1HtE2YHNE7rm804K6GeNJICLCjVTnXZ5rjyC5QOA130_provenance.
- NP90855.RAjjh1HtE2YHNE7rm804K6GeNJICLCjVTnXZ5rjyC5QOA130_assertion wasGeneratedBy ECO_0000203 NP90855.RAjjh1HtE2YHNE7rm804K6GeNJICLCjVTnXZ5rjyC5QOA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP90855.RAjjh1HtE2YHNE7rm804K6GeNJICLCjVTnXZ5rjyC5QOA130_provenance.