Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP385758.RAFgud6lXADII1yWVL5w_zwLeIqYvftp_wMN__fDBl0sA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP385758.RAFgud6lXADII1yWVL5w_zwLeIqYvftp_wMN__fDBl0sA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP385758.RAFgud6lXADII1yWVL5w_zwLeIqYvftp_wMN__fDBl0sA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP385758.RAFgud6lXADII1yWVL5w_zwLeIqYvftp_wMN__fDBl0sA130_provenance.
- NP385758.RAFgud6lXADII1yWVL5w_zwLeIqYvftp_wMN__fDBl0sA130_assertion description "[SRY gene is present in our BCA patients as well as in normal boys, and therefore BCA does not seem related to an anomaly of the opening reading frame sequence of the SRY gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP385758.RAFgud6lXADII1yWVL5w_zwLeIqYvftp_wMN__fDBl0sA130_provenance.
- NP385758.RAFgud6lXADII1yWVL5w_zwLeIqYvftp_wMN__fDBl0sA130_assertion evidence source_evidence_literature NP385758.RAFgud6lXADII1yWVL5w_zwLeIqYvftp_wMN__fDBl0sA130_provenance.
- NP385758.RAFgud6lXADII1yWVL5w_zwLeIqYvftp_wMN__fDBl0sA130_assertion SIO_000772 10584191 NP385758.RAFgud6lXADII1yWVL5w_zwLeIqYvftp_wMN__fDBl0sA130_provenance.
- NP385758.RAFgud6lXADII1yWVL5w_zwLeIqYvftp_wMN__fDBl0sA130_assertion wasDerivedFrom befree-20140225 NP385758.RAFgud6lXADII1yWVL5w_zwLeIqYvftp_wMN__fDBl0sA130_provenance.
- NP385758.RAFgud6lXADII1yWVL5w_zwLeIqYvftp_wMN__fDBl0sA130_assertion wasGeneratedBy ECO_0000203 NP385758.RAFgud6lXADII1yWVL5w_zwLeIqYvftp_wMN__fDBl0sA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP385758.RAFgud6lXADII1yWVL5w_zwLeIqYvftp_wMN__fDBl0sA130_provenance.