Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7219.RANSvDhvXIEB9iSxe9PvQAYVdMTnd6qUvH_0xqSZWcGqw130_assertion> ?p ?o ?g. }
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- NP7219.RANSvDhvXIEB9iSxe9PvQAYVdMTnd6qUvH_0xqSZWcGqw130_assertion type Assertion NP7219.RANSvDhvXIEB9iSxe9PvQAYVdMTnd6qUvH_0xqSZWcGqw130_head.
- NP7219.RANSvDhvXIEB9iSxe9PvQAYVdMTnd6qUvH_0xqSZWcGqw130_assertion description "[A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7219.RANSvDhvXIEB9iSxe9PvQAYVdMTnd6qUvH_0xqSZWcGqw130_provenance.
- NP7219.RANSvDhvXIEB9iSxe9PvQAYVdMTnd6qUvH_0xqSZWcGqw130_assertion evidence source_evidence_curated NP7219.RANSvDhvXIEB9iSxe9PvQAYVdMTnd6qUvH_0xqSZWcGqw130_provenance.
- NP7219.RANSvDhvXIEB9iSxe9PvQAYVdMTnd6qUvH_0xqSZWcGqw130_assertion SIO_000772 23000143 NP7219.RANSvDhvXIEB9iSxe9PvQAYVdMTnd6qUvH_0xqSZWcGqw130_provenance.
- NP7219.RANSvDhvXIEB9iSxe9PvQAYVdMTnd6qUvH_0xqSZWcGqw130_assertion wasDerivedFrom uniprot-2016 NP7219.RANSvDhvXIEB9iSxe9PvQAYVdMTnd6qUvH_0xqSZWcGqw130_provenance.
- NP7219.RANSvDhvXIEB9iSxe9PvQAYVdMTnd6qUvH_0xqSZWcGqw130_assertion wasGeneratedBy ECO_0000218 NP7219.RANSvDhvXIEB9iSxe9PvQAYVdMTnd6qUvH_0xqSZWcGqw130_provenance.