Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP835662.RAAlQa64OO--_6QoL_dsiTL1cOfGWzc7oAtljyNmwdS6E130_assertion> ?p ?o ?g. }
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- NP835662.RAAlQa64OO--_6QoL_dsiTL1cOfGWzc7oAtljyNmwdS6E130_assertion type Assertion NP835662.RAAlQa64OO--_6QoL_dsiTL1cOfGWzc7oAtljyNmwdS6E130_head.
- NP835662.RAAlQa64OO--_6QoL_dsiTL1cOfGWzc7oAtljyNmwdS6E130_assertion description "[Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835662.RAAlQa64OO--_6QoL_dsiTL1cOfGWzc7oAtljyNmwdS6E130_provenance.
- NP835662.RAAlQa64OO--_6QoL_dsiTL1cOfGWzc7oAtljyNmwdS6E130_assertion evidence source_evidence_literature NP835662.RAAlQa64OO--_6QoL_dsiTL1cOfGWzc7oAtljyNmwdS6E130_provenance.
- NP835662.RAAlQa64OO--_6QoL_dsiTL1cOfGWzc7oAtljyNmwdS6E130_assertion SIO_000772 20817137 NP835662.RAAlQa64OO--_6QoL_dsiTL1cOfGWzc7oAtljyNmwdS6E130_provenance.
- NP835662.RAAlQa64OO--_6QoL_dsiTL1cOfGWzc7oAtljyNmwdS6E130_assertion wasDerivedFrom befree-20140225 NP835662.RAAlQa64OO--_6QoL_dsiTL1cOfGWzc7oAtljyNmwdS6E130_provenance.
- NP835662.RAAlQa64OO--_6QoL_dsiTL1cOfGWzc7oAtljyNmwdS6E130_assertion wasGeneratedBy ECO_0000203 NP835662.RAAlQa64OO--_6QoL_dsiTL1cOfGWzc7oAtljyNmwdS6E130_provenance.