Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP318831.RA7_b5A6Wx9JqDnOZ7b21Na73QUXhhoR0HRRmy84LKcsM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP318831.RA7_b5A6Wx9JqDnOZ7b21Na73QUXhhoR0HRRmy84LKcsM130_assertion type Assertion NP318831.RA7_b5A6Wx9JqDnOZ7b21Na73QUXhhoR0HRRmy84LKcsM130_head.
- NP318831.RA7_b5A6Wx9JqDnOZ7b21Na73QUXhhoR0HRRmy84LKcsM130_assertion wasGeneratedBy ECO_0000203 NP318831.RA7_b5A6Wx9JqDnOZ7b21Na73QUXhhoR0HRRmy84LKcsM130_provenance.
- NP318831.RA7_b5A6Wx9JqDnOZ7b21Na73QUXhhoR0HRRmy84LKcsM130_assertion wasDerivedFrom befree-20140225 NP318831.RA7_b5A6Wx9JqDnOZ7b21Na73QUXhhoR0HRRmy84LKcsM130_provenance.
- NP318831.RA7_b5A6Wx9JqDnOZ7b21Na73QUXhhoR0HRRmy84LKcsM130_assertion SIO_000772 23228431 NP318831.RA7_b5A6Wx9JqDnOZ7b21Na73QUXhhoR0HRRmy84LKcsM130_provenance.
- NP318831.RA7_b5A6Wx9JqDnOZ7b21Na73QUXhhoR0HRRmy84LKcsM130_assertion evidence source_evidence_literature NP318831.RA7_b5A6Wx9JqDnOZ7b21Na73QUXhhoR0HRRmy84LKcsM130_provenance.
- NP318831.RA7_b5A6Wx9JqDnOZ7b21Na73QUXhhoR0HRRmy84LKcsM130_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." NP318831.RA7_b5A6Wx9JqDnOZ7b21Na73QUXhhoR0HRRmy84LKcsM130_provenance.