Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP981266.RAYCCzJ8piv4Znk5NUlFvNZoHSOZMvCqCOyO4rx9Y7vLs130_assertion> ?p ?o ?g. }
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- NP981266.RAYCCzJ8piv4Znk5NUlFvNZoHSOZMvCqCOyO4rx9Y7vLs130_assertion type Assertion NP981266.RAYCCzJ8piv4Znk5NUlFvNZoHSOZMvCqCOyO4rx9Y7vLs130_head.
- NP981266.RAYCCzJ8piv4Znk5NUlFvNZoHSOZMvCqCOyO4rx9Y7vLs130_assertion description "[Therefore, the authors' data provide supportive evidence that mutations in the coding region of the NKX2-5 gene and sequence variants within its promoter region may be among the contributors to the CHD etiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP981266.RAYCCzJ8piv4Znk5NUlFvNZoHSOZMvCqCOyO4rx9Y7vLs130_provenance.
- NP981266.RAYCCzJ8piv4Znk5NUlFvNZoHSOZMvCqCOyO4rx9Y7vLs130_assertion evidence source_evidence_literature NP981266.RAYCCzJ8piv4Znk5NUlFvNZoHSOZMvCqCOyO4rx9Y7vLs130_provenance.
- NP981266.RAYCCzJ8piv4Znk5NUlFvNZoHSOZMvCqCOyO4rx9Y7vLs130_assertion SIO_000772 22576768 NP981266.RAYCCzJ8piv4Znk5NUlFvNZoHSOZMvCqCOyO4rx9Y7vLs130_provenance.
- NP981266.RAYCCzJ8piv4Znk5NUlFvNZoHSOZMvCqCOyO4rx9Y7vLs130_assertion wasDerivedFrom befree-2016 NP981266.RAYCCzJ8piv4Znk5NUlFvNZoHSOZMvCqCOyO4rx9Y7vLs130_provenance.
- NP981266.RAYCCzJ8piv4Znk5NUlFvNZoHSOZMvCqCOyO4rx9Y7vLs130_assertion wasGeneratedBy ECO_0000203 NP981266.RAYCCzJ8piv4Znk5NUlFvNZoHSOZMvCqCOyO4rx9Y7vLs130_provenance.