Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP87913.RAjth6msSGDrqQYxLz0gev940d_WnovBXE-oEZh7t6AXI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP87913.RAjth6msSGDrqQYxLz0gev940d_WnovBXE-oEZh7t6AXI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP87913.RAjth6msSGDrqQYxLz0gev940d_WnovBXE-oEZh7t6AXI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP87913.RAjth6msSGDrqQYxLz0gev940d_WnovBXE-oEZh7t6AXI130_provenance.
- NP87913.RAjth6msSGDrqQYxLz0gev940d_WnovBXE-oEZh7t6AXI130_assertion description "[Modest associations were observed in CITED2, EP300, CREBBP, TFAP2A and CARM1 but not ALX1. However, these modest associations were not statistically significant after correction for multiple comparisons. Searching for potential functional variants and rare causal mutations is warranted in these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87913.RAjth6msSGDrqQYxLz0gev940d_WnovBXE-oEZh7t6AXI130_provenance.
- NP87913.RAjth6msSGDrqQYxLz0gev940d_WnovBXE-oEZh7t6AXI130_assertion evidence source_evidence_literature NP87913.RAjth6msSGDrqQYxLz0gev940d_WnovBXE-oEZh7t6AXI130_provenance.
- NP87913.RAjth6msSGDrqQYxLz0gev940d_WnovBXE-oEZh7t6AXI130_assertion SIO_000772 20932315 NP87913.RAjth6msSGDrqQYxLz0gev940d_WnovBXE-oEZh7t6AXI130_provenance.
- NP87913.RAjth6msSGDrqQYxLz0gev940d_WnovBXE-oEZh7t6AXI130_assertion wasDerivedFrom gad-20130706 NP87913.RAjth6msSGDrqQYxLz0gev940d_WnovBXE-oEZh7t6AXI130_provenance.
- NP87913.RAjth6msSGDrqQYxLz0gev940d_WnovBXE-oEZh7t6AXI130_assertion wasGeneratedBy ECO_0000203 NP87913.RAjth6msSGDrqQYxLz0gev940d_WnovBXE-oEZh7t6AXI130_provenance.
- gad-20130706 importedOn "2013-07-06" NP87913.RAjth6msSGDrqQYxLz0gev940d_WnovBXE-oEZh7t6AXI130_provenance.