Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP29656.RAwwJNCXepn35QvUYti91tGuBWf8F1W_nDT_2OJDqVhrc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP29656.RAwwJNCXepn35QvUYti91tGuBWf8F1W_nDT_2OJDqVhrc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP29656.RAwwJNCXepn35QvUYti91tGuBWf8F1W_nDT_2OJDqVhrc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP29656.RAwwJNCXepn35QvUYti91tGuBWf8F1W_nDT_2OJDqVhrc130_provenance.
- NP29656.RAwwJNCXepn35QvUYti91tGuBWf8F1W_nDT_2OJDqVhrc130_assertion description "[Functional impact of global rare copy number variation in autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29656.RAwwJNCXepn35QvUYti91tGuBWf8F1W_nDT_2OJDqVhrc130_provenance.
- NP29656.RAwwJNCXepn35QvUYti91tGuBWf8F1W_nDT_2OJDqVhrc130_assertion evidence source_evidence_curated NP29656.RAwwJNCXepn35QvUYti91tGuBWf8F1W_nDT_2OJDqVhrc130_provenance.
- NP29656.RAwwJNCXepn35QvUYti91tGuBWf8F1W_nDT_2OJDqVhrc130_assertion SIO_000772 20531469 NP29656.RAwwJNCXepn35QvUYti91tGuBWf8F1W_nDT_2OJDqVhrc130_provenance.
- NP29656.RAwwJNCXepn35QvUYti91tGuBWf8F1W_nDT_2OJDqVhrc130_assertion wasDerivedFrom ctd_human-20150221 NP29656.RAwwJNCXepn35QvUYti91tGuBWf8F1W_nDT_2OJDqVhrc130_provenance.
- NP29656.RAwwJNCXepn35QvUYti91tGuBWf8F1W_nDT_2OJDqVhrc130_assertion wasGeneratedBy ECO_0000218 NP29656.RAwwJNCXepn35QvUYti91tGuBWf8F1W_nDT_2OJDqVhrc130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP29656.RAwwJNCXepn35QvUYti91tGuBWf8F1W_nDT_2OJDqVhrc130_provenance.