Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP23967.RAnJyfDbiGlq3nQH0DjU0vOXsWAQyG_V_t05NiOO5bMb0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP23967.RAnJyfDbiGlq3nQH0DjU0vOXsWAQyG_V_t05NiOO5bMb0130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP23967.RAnJyfDbiGlq3nQH0DjU0vOXsWAQyG_V_t05NiOO5bMb0130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP23967.RAnJyfDbiGlq3nQH0DjU0vOXsWAQyG_V_t05NiOO5bMb0130_provenance.
- NP23967.RAnJyfDbiGlq3nQH0DjU0vOXsWAQyG_V_t05NiOO5bMb0130_assertion description "[High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP23967.RAnJyfDbiGlq3nQH0DjU0vOXsWAQyG_V_t05NiOO5bMb0130_provenance.
- NP23967.RAnJyfDbiGlq3nQH0DjU0vOXsWAQyG_V_t05NiOO5bMb0130_assertion evidence source_evidence_curated NP23967.RAnJyfDbiGlq3nQH0DjU0vOXsWAQyG_V_t05NiOO5bMb0130_provenance.
- NP23967.RAnJyfDbiGlq3nQH0DjU0vOXsWAQyG_V_t05NiOO5bMb0130_assertion SIO_000772 19401682 NP23967.RAnJyfDbiGlq3nQH0DjU0vOXsWAQyG_V_t05NiOO5bMb0130_provenance.
- NP23967.RAnJyfDbiGlq3nQH0DjU0vOXsWAQyG_V_t05NiOO5bMb0130_assertion wasDerivedFrom ctd_human-2016 NP23967.RAnJyfDbiGlq3nQH0DjU0vOXsWAQyG_V_t05NiOO5bMb0130_provenance.
- NP23967.RAnJyfDbiGlq3nQH0DjU0vOXsWAQyG_V_t05NiOO5bMb0130_assertion wasGeneratedBy ECO_0000218 NP23967.RAnJyfDbiGlq3nQH0DjU0vOXsWAQyG_V_t05NiOO5bMb0130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP23967.RAnJyfDbiGlq3nQH0DjU0vOXsWAQyG_V_t05NiOO5bMb0130_provenance.