Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP685904.RAjbDMNVgiWnL7ugF8z-FG8Kr1rXO0iwLxx1IpRB_KGuY130_assertion> ?p ?o ?g. }
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- NP685904.RAjbDMNVgiWnL7ugF8z-FG8Kr1rXO0iwLxx1IpRB_KGuY130_assertion type Assertion NP685904.RAjbDMNVgiWnL7ugF8z-FG8Kr1rXO0iwLxx1IpRB_KGuY130_head.
- NP685904.RAjbDMNVgiWnL7ugF8z-FG8Kr1rXO0iwLxx1IpRB_KGuY130_assertion wasGeneratedBy ECO_0000203 NP685904.RAjbDMNVgiWnL7ugF8z-FG8Kr1rXO0iwLxx1IpRB_KGuY130_provenance.
- NP685904.RAjbDMNVgiWnL7ugF8z-FG8Kr1rXO0iwLxx1IpRB_KGuY130_assertion wasDerivedFrom befree-20140225 NP685904.RAjbDMNVgiWnL7ugF8z-FG8Kr1rXO0iwLxx1IpRB_KGuY130_provenance.
- NP685904.RAjbDMNVgiWnL7ugF8z-FG8Kr1rXO0iwLxx1IpRB_KGuY130_assertion SIO_000772 23228431 NP685904.RAjbDMNVgiWnL7ugF8z-FG8Kr1rXO0iwLxx1IpRB_KGuY130_provenance.
- NP685904.RAjbDMNVgiWnL7ugF8z-FG8Kr1rXO0iwLxx1IpRB_KGuY130_assertion evidence source_evidence_literature NP685904.RAjbDMNVgiWnL7ugF8z-FG8Kr1rXO0iwLxx1IpRB_KGuY130_provenance.
- NP685904.RAjbDMNVgiWnL7ugF8z-FG8Kr1rXO0iwLxx1IpRB_KGuY130_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." NP685904.RAjbDMNVgiWnL7ugF8z-FG8Kr1rXO0iwLxx1IpRB_KGuY130_provenance.