Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_provenance.
- NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_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." NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_provenance.
- NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_assertion evidence source_evidence_literature NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_provenance.
- NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_assertion SIO_000772 16684826 NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_provenance.
- NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_assertion wasDerivedFrom befree-20140225 NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_provenance.
- NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_assertion wasGeneratedBy ECO_0000203 NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_provenance.