Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP54651.RAKBN_i9eER-EIf7wRyKDOAMJ0gA9nlMfEGopGIqMKRXI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP54651.RAKBN_i9eER-EIf7wRyKDOAMJ0gA9nlMfEGopGIqMKRXI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP54651.RAKBN_i9eER-EIf7wRyKDOAMJ0gA9nlMfEGopGIqMKRXI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP54651.RAKBN_i9eER-EIf7wRyKDOAMJ0gA9nlMfEGopGIqMKRXI130_provenance.
- NP54651.RAKBN_i9eER-EIf7wRyKDOAMJ0gA9nlMfEGopGIqMKRXI130_assertion description "[Common genetic variants on 1p13.2 associate with risk of autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54651.RAKBN_i9eER-EIf7wRyKDOAMJ0gA9nlMfEGopGIqMKRXI130_provenance.
- NP54651.RAKBN_i9eER-EIf7wRyKDOAMJ0gA9nlMfEGopGIqMKRXI130_assertion evidence source_evidence_curated NP54651.RAKBN_i9eER-EIf7wRyKDOAMJ0gA9nlMfEGopGIqMKRXI130_provenance.
- NP54651.RAKBN_i9eER-EIf7wRyKDOAMJ0gA9nlMfEGopGIqMKRXI130_assertion SIO_000772 24189344 NP54651.RAKBN_i9eER-EIf7wRyKDOAMJ0gA9nlMfEGopGIqMKRXI130_provenance.
- NP54651.RAKBN_i9eER-EIf7wRyKDOAMJ0gA9nlMfEGopGIqMKRXI130_assertion wasDerivedFrom gwascat-2016 NP54651.RAKBN_i9eER-EIf7wRyKDOAMJ0gA9nlMfEGopGIqMKRXI130_provenance.
- NP54651.RAKBN_i9eER-EIf7wRyKDOAMJ0gA9nlMfEGopGIqMKRXI130_assertion wasGeneratedBy ECO_0000218 NP54651.RAKBN_i9eER-EIf7wRyKDOAMJ0gA9nlMfEGopGIqMKRXI130_provenance.
- gwascat-2016 importedOn "2016-01-27" NP54651.RAKBN_i9eER-EIf7wRyKDOAMJ0gA9nlMfEGopGIqMKRXI130_provenance.