Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP836309.RAoffbwD3V9yKGE5wM1w__sCIFwfkx8TcbIxIzoGWQg5g130_assertion> ?p ?o ?g. }
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- NP836309.RAoffbwD3V9yKGE5wM1w__sCIFwfkx8TcbIxIzoGWQg5g130_assertion type Assertion NP836309.RAoffbwD3V9yKGE5wM1w__sCIFwfkx8TcbIxIzoGWQg5g130_head.
- NP836309.RAoffbwD3V9yKGE5wM1w__sCIFwfkx8TcbIxIzoGWQg5g130_assertion description "[These data provide a proof-of-concept that the catalogue of p63 binding sites identified in this study may be of relevance to the studies of SHFM and other congenital malformations that resemble the p63-associated phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836309.RAoffbwD3V9yKGE5wM1w__sCIFwfkx8TcbIxIzoGWQg5g130_provenance.
- NP836309.RAoffbwD3V9yKGE5wM1w__sCIFwfkx8TcbIxIzoGWQg5g130_assertion evidence source_evidence_literature NP836309.RAoffbwD3V9yKGE5wM1w__sCIFwfkx8TcbIxIzoGWQg5g130_provenance.
- NP836309.RAoffbwD3V9yKGE5wM1w__sCIFwfkx8TcbIxIzoGWQg5g130_assertion SIO_000772 20808887 NP836309.RAoffbwD3V9yKGE5wM1w__sCIFwfkx8TcbIxIzoGWQg5g130_provenance.
- NP836309.RAoffbwD3V9yKGE5wM1w__sCIFwfkx8TcbIxIzoGWQg5g130_assertion wasDerivedFrom befree-2016 NP836309.RAoffbwD3V9yKGE5wM1w__sCIFwfkx8TcbIxIzoGWQg5g130_provenance.
- NP836309.RAoffbwD3V9yKGE5wM1w__sCIFwfkx8TcbIxIzoGWQg5g130_assertion wasGeneratedBy ECO_0000203 NP836309.RAoffbwD3V9yKGE5wM1w__sCIFwfkx8TcbIxIzoGWQg5g130_provenance.