Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_assertion type Assertion NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_head.
- NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_assertion description "[The contribution of copy number variation (CNV) to specific congenital heart disease (CHD) phenotypes including AVSD is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_provenance.
- NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_assertion evidence source_evidence_literature NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_provenance.
- NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_assertion SIO_000772 22529060 NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_provenance.
- NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_assertion wasDerivedFrom befree-2016 NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_provenance.
- NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_assertion wasGeneratedBy ECO_0000203 NP977085.RA4gbviKrF-Hj8-GFH0mEIRs_KJ8BhF6naJ71aNa4oKyI130_provenance.