Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_assertion> ?p ?o ?g. }
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- NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_assertion type Assertion NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_head.
- NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_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." NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_provenance.
- NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_assertion evidence source_evidence_literature NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_provenance.
- NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_assertion SIO_000772 22529060 NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_provenance.
- NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_assertion wasDerivedFrom befree-20150227 NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_provenance.
- NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_assertion wasGeneratedBy ECO_0000203 NP775756.RAuqH-1p1hXUQpe-BgkgbpL3oOw0HwhJe8yujG1NuXavw130_provenance.