Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP915059.RAC1jrZMR2sq7cITtZljzRZaFsDDWPCi9Ql29uplIcHhQ130_assertion> ?p ?o ?g. }
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- NP915059.RAC1jrZMR2sq7cITtZljzRZaFsDDWPCi9Ql29uplIcHhQ130_assertion type Assertion NP915059.RAC1jrZMR2sq7cITtZljzRZaFsDDWPCi9Ql29uplIcHhQ130_head.
- NP915059.RAC1jrZMR2sq7cITtZljzRZaFsDDWPCi9Ql29uplIcHhQ130_assertion description "[WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915059.RAC1jrZMR2sq7cITtZljzRZaFsDDWPCi9Ql29uplIcHhQ130_provenance.
- NP915059.RAC1jrZMR2sq7cITtZljzRZaFsDDWPCi9Ql29uplIcHhQ130_assertion evidence source_evidence_literature NP915059.RAC1jrZMR2sq7cITtZljzRZaFsDDWPCi9Ql29uplIcHhQ130_provenance.
- NP915059.RAC1jrZMR2sq7cITtZljzRZaFsDDWPCi9Ql29uplIcHhQ130_assertion SIO_000772 19559398 NP915059.RAC1jrZMR2sq7cITtZljzRZaFsDDWPCi9Ql29uplIcHhQ130_provenance.
- NP915059.RAC1jrZMR2sq7cITtZljzRZaFsDDWPCi9Ql29uplIcHhQ130_assertion wasDerivedFrom befree-20140225 NP915059.RAC1jrZMR2sq7cITtZljzRZaFsDDWPCi9Ql29uplIcHhQ130_provenance.
- NP915059.RAC1jrZMR2sq7cITtZljzRZaFsDDWPCi9Ql29uplIcHhQ130_assertion wasGeneratedBy ECO_0000203 NP915059.RAC1jrZMR2sq7cITtZljzRZaFsDDWPCi9Ql29uplIcHhQ130_provenance.