Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP695459.RAxUtMQrpDTNuXN3BuGIpHt7zGGNlnmyq--J9Fxd_tVtc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP695459.RAxUtMQrpDTNuXN3BuGIpHt7zGGNlnmyq--J9Fxd_tVtc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP695459.RAxUtMQrpDTNuXN3BuGIpHt7zGGNlnmyq--J9Fxd_tVtc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP695459.RAxUtMQrpDTNuXN3BuGIpHt7zGGNlnmyq--J9Fxd_tVtc130_provenance.
- NP695459.RAxUtMQrpDTNuXN3BuGIpHt7zGGNlnmyq--J9Fxd_tVtc130_assertion description "[Mutations in the Aristaless-related homeobox (ARX) gene are associated with pleiotropic phenotypes including infantile spasms, mental retardation and dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695459.RAxUtMQrpDTNuXN3BuGIpHt7zGGNlnmyq--J9Fxd_tVtc130_provenance.
- NP695459.RAxUtMQrpDTNuXN3BuGIpHt7zGGNlnmyq--J9Fxd_tVtc130_assertion evidence source_evidence_literature NP695459.RAxUtMQrpDTNuXN3BuGIpHt7zGGNlnmyq--J9Fxd_tVtc130_provenance.
- NP695459.RAxUtMQrpDTNuXN3BuGIpHt7zGGNlnmyq--J9Fxd_tVtc130_assertion SIO_000772 18823727 NP695459.RAxUtMQrpDTNuXN3BuGIpHt7zGGNlnmyq--J9Fxd_tVtc130_provenance.
- NP695459.RAxUtMQrpDTNuXN3BuGIpHt7zGGNlnmyq--J9Fxd_tVtc130_assertion wasDerivedFrom befree-2016 NP695459.RAxUtMQrpDTNuXN3BuGIpHt7zGGNlnmyq--J9Fxd_tVtc130_provenance.
- NP695459.RAxUtMQrpDTNuXN3BuGIpHt7zGGNlnmyq--J9Fxd_tVtc130_assertion wasGeneratedBy ECO_0000203 NP695459.RAxUtMQrpDTNuXN3BuGIpHt7zGGNlnmyq--J9Fxd_tVtc130_provenance.
- befree-2016 importedOn "2016-02-19" NP695459.RAxUtMQrpDTNuXN3BuGIpHt7zGGNlnmyq--J9Fxd_tVtc130_provenance.