Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP302082.RAlyBEzm80byBWN_sGidpz2xi7Q43D_s6H89dEYHewe2c130_assertion> ?p ?o ?g. }
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- NP302082.RAlyBEzm80byBWN_sGidpz2xi7Q43D_s6H89dEYHewe2c130_assertion type Assertion NP302082.RAlyBEzm80byBWN_sGidpz2xi7Q43D_s6H89dEYHewe2c130_head.
- NP302082.RAlyBEzm80byBWN_sGidpz2xi7Q43D_s6H89dEYHewe2c130_assertion description "[Rare mutations affecting the FOXP2 transcription factor cause a monogenic speech and language disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP302082.RAlyBEzm80byBWN_sGidpz2xi7Q43D_s6H89dEYHewe2c130_provenance.
- NP302082.RAlyBEzm80byBWN_sGidpz2xi7Q43D_s6H89dEYHewe2c130_assertion evidence source_evidence_literature NP302082.RAlyBEzm80byBWN_sGidpz2xi7Q43D_s6H89dEYHewe2c130_provenance.
- NP302082.RAlyBEzm80byBWN_sGidpz2xi7Q43D_s6H89dEYHewe2c130_assertion SIO_000772 18987363 NP302082.RAlyBEzm80byBWN_sGidpz2xi7Q43D_s6H89dEYHewe2c130_provenance.
- NP302082.RAlyBEzm80byBWN_sGidpz2xi7Q43D_s6H89dEYHewe2c130_assertion wasDerivedFrom befree-20140225 NP302082.RAlyBEzm80byBWN_sGidpz2xi7Q43D_s6H89dEYHewe2c130_provenance.
- NP302082.RAlyBEzm80byBWN_sGidpz2xi7Q43D_s6H89dEYHewe2c130_assertion wasGeneratedBy ECO_0000203 NP302082.RAlyBEzm80byBWN_sGidpz2xi7Q43D_s6H89dEYHewe2c130_provenance.