Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1035059.RAxPz1YWztWwmKTbs9FA0gYE-g3jI69KCEnvJzXwMtPpY130_assertion> ?p ?o ?g. }
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- NP1035059.RAxPz1YWztWwmKTbs9FA0gYE-g3jI69KCEnvJzXwMtPpY130_assertion type Assertion NP1035059.RAxPz1YWztWwmKTbs9FA0gYE-g3jI69KCEnvJzXwMtPpY130_head.
- NP1035059.RAxPz1YWztWwmKTbs9FA0gYE-g3jI69KCEnvJzXwMtPpY130_assertion description "[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1035059.RAxPz1YWztWwmKTbs9FA0gYE-g3jI69KCEnvJzXwMtPpY130_provenance.
- NP1035059.RAxPz1YWztWwmKTbs9FA0gYE-g3jI69KCEnvJzXwMtPpY130_assertion evidence source_evidence_literature NP1035059.RAxPz1YWztWwmKTbs9FA0gYE-g3jI69KCEnvJzXwMtPpY130_provenance.
- NP1035059.RAxPz1YWztWwmKTbs9FA0gYE-g3jI69KCEnvJzXwMtPpY130_assertion SIO_000772 23228431 NP1035059.RAxPz1YWztWwmKTbs9FA0gYE-g3jI69KCEnvJzXwMtPpY130_provenance.
- NP1035059.RAxPz1YWztWwmKTbs9FA0gYE-g3jI69KCEnvJzXwMtPpY130_assertion wasDerivedFrom befree-2016 NP1035059.RAxPz1YWztWwmKTbs9FA0gYE-g3jI69KCEnvJzXwMtPpY130_provenance.
- NP1035059.RAxPz1YWztWwmKTbs9FA0gYE-g3jI69KCEnvJzXwMtPpY130_assertion wasGeneratedBy ECO_0000203 NP1035059.RAxPz1YWztWwmKTbs9FA0gYE-g3jI69KCEnvJzXwMtPpY130_provenance.