Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP564706.RA-9hE7u_bcnZlqCpHIIrQ2M9CFGAXHGqBIV6Lsl3xRDg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP564706.RA-9hE7u_bcnZlqCpHIIrQ2M9CFGAXHGqBIV6Lsl3xRDg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP564706.RA-9hE7u_bcnZlqCpHIIrQ2M9CFGAXHGqBIV6Lsl3xRDg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP564706.RA-9hE7u_bcnZlqCpHIIrQ2M9CFGAXHGqBIV6Lsl3xRDg130_provenance.
- NP564706.RA-9hE7u_bcnZlqCpHIIrQ2M9CFGAXHGqBIV6Lsl3xRDg130_assertion description "[Our study illustrates that if only a single heterozygous SLC26A4/PDS mutation is found in a patient with goiter and deafness, other genetic explanations should be considered.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP564706.RA-9hE7u_bcnZlqCpHIIrQ2M9CFGAXHGqBIV6Lsl3xRDg130_provenance.
- NP564706.RA-9hE7u_bcnZlqCpHIIrQ2M9CFGAXHGqBIV6Lsl3xRDg130_assertion evidence source_evidence_literature NP564706.RA-9hE7u_bcnZlqCpHIIrQ2M9CFGAXHGqBIV6Lsl3xRDg130_provenance.
- NP564706.RA-9hE7u_bcnZlqCpHIIrQ2M9CFGAXHGqBIV6Lsl3xRDg130_assertion SIO_000772 16684826 NP564706.RA-9hE7u_bcnZlqCpHIIrQ2M9CFGAXHGqBIV6Lsl3xRDg130_provenance.
- NP564706.RA-9hE7u_bcnZlqCpHIIrQ2M9CFGAXHGqBIV6Lsl3xRDg130_assertion wasDerivedFrom befree-20140225 NP564706.RA-9hE7u_bcnZlqCpHIIrQ2M9CFGAXHGqBIV6Lsl3xRDg130_provenance.
- NP564706.RA-9hE7u_bcnZlqCpHIIrQ2M9CFGAXHGqBIV6Lsl3xRDg130_assertion wasGeneratedBy ECO_0000203 NP564706.RA-9hE7u_bcnZlqCpHIIrQ2M9CFGAXHGqBIV6Lsl3xRDg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP564706.RA-9hE7u_bcnZlqCpHIIrQ2M9CFGAXHGqBIV6Lsl3xRDg130_provenance.