Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP915059.RAC1jrZMR2sq7cITtZljzRZaFsDDWPCi9Ql29uplIcHhQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP915059.RAC1jrZMR2sq7cITtZljzRZaFsDDWPCi9Ql29uplIcHhQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP915059.RAC1jrZMR2sq7cITtZljzRZaFsDDWPCi9Ql29uplIcHhQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP915059.RAC1jrZMR2sq7cITtZljzRZaFsDDWPCi9Ql29uplIcHhQ130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP915059.RAC1jrZMR2sq7cITtZljzRZaFsDDWPCi9Ql29uplIcHhQ130_provenance.