Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP941702.RAAuMr2CDYvHRN5zaisz8q0bKwkl2uQdFFPItB5QgA-UU130_assertion> ?p ?o ?g. }
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- NP941702.RAAuMr2CDYvHRN5zaisz8q0bKwkl2uQdFFPItB5QgA-UU130_assertion type Assertion NP941702.RAAuMr2CDYvHRN5zaisz8q0bKwkl2uQdFFPItB5QgA-UU130_head.
- NP941702.RAAuMr2CDYvHRN5zaisz8q0bKwkl2uQdFFPItB5QgA-UU130_assertion description "[Analysis of the CRELD1 gene from individuals with non-trisomy 21-associated AVSD identified heterozygous missense mutations in nearly 6% of this population, including mutations in isolated AVSD and AVSD associated with heterotaxy syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP941702.RAAuMr2CDYvHRN5zaisz8q0bKwkl2uQdFFPItB5QgA-UU130_provenance.
- NP941702.RAAuMr2CDYvHRN5zaisz8q0bKwkl2uQdFFPItB5QgA-UU130_assertion evidence source_evidence_literature NP941702.RAAuMr2CDYvHRN5zaisz8q0bKwkl2uQdFFPItB5QgA-UU130_provenance.
- NP941702.RAAuMr2CDYvHRN5zaisz8q0bKwkl2uQdFFPItB5QgA-UU130_assertion SIO_000772 12632326 NP941702.RAAuMr2CDYvHRN5zaisz8q0bKwkl2uQdFFPItB5QgA-UU130_provenance.
- NP941702.RAAuMr2CDYvHRN5zaisz8q0bKwkl2uQdFFPItB5QgA-UU130_assertion wasDerivedFrom befree-20150227 NP941702.RAAuMr2CDYvHRN5zaisz8q0bKwkl2uQdFFPItB5QgA-UU130_provenance.
- NP941702.RAAuMr2CDYvHRN5zaisz8q0bKwkl2uQdFFPItB5QgA-UU130_assertion wasGeneratedBy ECO_0000203 NP941702.RAAuMr2CDYvHRN5zaisz8q0bKwkl2uQdFFPItB5QgA-UU130_provenance.