Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP527764.RA2ds79FmaUdK14o981O2NwozAmJS36SnLYrjgnSl2g5Q130_assertion> ?p ?o ?g. }
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- NP527764.RA2ds79FmaUdK14o981O2NwozAmJS36SnLYrjgnSl2g5Q130_assertion type Assertion NP527764.RA2ds79FmaUdK14o981O2NwozAmJS36SnLYrjgnSl2g5Q130_head.
- NP527764.RA2ds79FmaUdK14o981O2NwozAmJS36SnLYrjgnSl2g5Q130_assertion wasGeneratedBy ECO_0000203 NP527764.RA2ds79FmaUdK14o981O2NwozAmJS36SnLYrjgnSl2g5Q130_provenance.
- NP527764.RA2ds79FmaUdK14o981O2NwozAmJS36SnLYrjgnSl2g5Q130_assertion wasDerivedFrom befree-20140225 NP527764.RA2ds79FmaUdK14o981O2NwozAmJS36SnLYrjgnSl2g5Q130_provenance.
- NP527764.RA2ds79FmaUdK14o981O2NwozAmJS36SnLYrjgnSl2g5Q130_assertion SIO_000772 15930903 NP527764.RA2ds79FmaUdK14o981O2NwozAmJS36SnLYrjgnSl2g5Q130_provenance.
- NP527764.RA2ds79FmaUdK14o981O2NwozAmJS36SnLYrjgnSl2g5Q130_assertion evidence source_evidence_literature NP527764.RA2ds79FmaUdK14o981O2NwozAmJS36SnLYrjgnSl2g5Q130_provenance.
- NP527764.RA2ds79FmaUdK14o981O2NwozAmJS36SnLYrjgnSl2g5Q130_assertion description "[The only other similar case with a deletion of 20p11.22-p11.23 exhibited a phenotype that also included abnormal neural development (autism, craniofacial dysmorphism, and Hirschsprung disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP527764.RA2ds79FmaUdK14o981O2NwozAmJS36SnLYrjgnSl2g5Q130_provenance.