Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP237742.RAU0XElsxcKmcc0qAZyRaJ9F_VYBuLsuMjmEfdpZxG7Pc130_assertion> ?p ?o ?g. }
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- NP237742.RAU0XElsxcKmcc0qAZyRaJ9F_VYBuLsuMjmEfdpZxG7Pc130_assertion type Assertion NP237742.RAU0XElsxcKmcc0qAZyRaJ9F_VYBuLsuMjmEfdpZxG7Pc130_head.
- NP237742.RAU0XElsxcKmcc0qAZyRaJ9F_VYBuLsuMjmEfdpZxG7Pc130_assertion description "[However, previous mutation analysis of the coding sequence of the HOX11L1 gene in patients affected with IND detected neither mutations nor other nucleotide variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237742.RAU0XElsxcKmcc0qAZyRaJ9F_VYBuLsuMjmEfdpZxG7Pc130_provenance.
- NP237742.RAU0XElsxcKmcc0qAZyRaJ9F_VYBuLsuMjmEfdpZxG7Pc130_assertion evidence source_evidence_literature NP237742.RAU0XElsxcKmcc0qAZyRaJ9F_VYBuLsuMjmEfdpZxG7Pc130_provenance.
- NP237742.RAU0XElsxcKmcc0qAZyRaJ9F_VYBuLsuMjmEfdpZxG7Pc130_assertion SIO_000772 12060859 NP237742.RAU0XElsxcKmcc0qAZyRaJ9F_VYBuLsuMjmEfdpZxG7Pc130_provenance.
- NP237742.RAU0XElsxcKmcc0qAZyRaJ9F_VYBuLsuMjmEfdpZxG7Pc130_assertion wasDerivedFrom befree-20140225 NP237742.RAU0XElsxcKmcc0qAZyRaJ9F_VYBuLsuMjmEfdpZxG7Pc130_provenance.
- NP237742.RAU0XElsxcKmcc0qAZyRaJ9F_VYBuLsuMjmEfdpZxG7Pc130_assertion wasGeneratedBy ECO_0000203 NP237742.RAU0XElsxcKmcc0qAZyRaJ9F_VYBuLsuMjmEfdpZxG7Pc130_provenance.