Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP985837.RApkVnkQTn6QKM0r8nn_mIUOtvpQLqsR8EI6D7yxDCFX8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP985837.RApkVnkQTn6QKM0r8nn_mIUOtvpQLqsR8EI6D7yxDCFX8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP985837.RApkVnkQTn6QKM0r8nn_mIUOtvpQLqsR8EI6D7yxDCFX8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP985837.RApkVnkQTn6QKM0r8nn_mIUOtvpQLqsR8EI6D7yxDCFX8130_provenance.
- NP985837.RApkVnkQTn6QKM0r8nn_mIUOtvpQLqsR8EI6D7yxDCFX8130_assertion description "[Interestingly, the patient with decreased KIAA2022 expression had only mild ID with severe language delay and repetitive behaviors falling in the range of an autism spectrum disorder (ASD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP985837.RApkVnkQTn6QKM0r8nn_mIUOtvpQLqsR8EI6D7yxDCFX8130_provenance.
- NP985837.RApkVnkQTn6QKM0r8nn_mIUOtvpQLqsR8EI6D7yxDCFX8130_assertion evidence source_evidence_literature NP985837.RApkVnkQTn6QKM0r8nn_mIUOtvpQLqsR8EI6D7yxDCFX8130_provenance.
- NP985837.RApkVnkQTn6QKM0r8nn_mIUOtvpQLqsR8EI6D7yxDCFX8130_assertion SIO_000772 23615299 NP985837.RApkVnkQTn6QKM0r8nn_mIUOtvpQLqsR8EI6D7yxDCFX8130_provenance.
- NP985837.RApkVnkQTn6QKM0r8nn_mIUOtvpQLqsR8EI6D7yxDCFX8130_assertion wasDerivedFrom befree-20150227 NP985837.RApkVnkQTn6QKM0r8nn_mIUOtvpQLqsR8EI6D7yxDCFX8130_provenance.
- NP985837.RApkVnkQTn6QKM0r8nn_mIUOtvpQLqsR8EI6D7yxDCFX8130_assertion wasGeneratedBy ECO_0000203 NP985837.RApkVnkQTn6QKM0r8nn_mIUOtvpQLqsR8EI6D7yxDCFX8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP985837.RApkVnkQTn6QKM0r8nn_mIUOtvpQLqsR8EI6D7yxDCFX8130_provenance.