Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP209006.RAW2M4tB5H5bNIJgAXH1wFNVaFN2Avi6q3qMQq1JdBvNE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP209006.RAW2M4tB5H5bNIJgAXH1wFNVaFN2Avi6q3qMQq1JdBvNE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP209006.RAW2M4tB5H5bNIJgAXH1wFNVaFN2Avi6q3qMQq1JdBvNE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP209006.RAW2M4tB5H5bNIJgAXH1wFNVaFN2Avi6q3qMQq1JdBvNE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP209006.RAW2M4tB5H5bNIJgAXH1wFNVaFN2Avi6q3qMQq1JdBvNE130_provenance.
- NP209006.RAW2M4tB5H5bNIJgAXH1wFNVaFN2Avi6q3qMQq1JdBvNE130_assertion wasGeneratedBy ECO_0000203 NP209006.RAW2M4tB5H5bNIJgAXH1wFNVaFN2Avi6q3qMQq1JdBvNE130_provenance.
- NP209006.RAW2M4tB5H5bNIJgAXH1wFNVaFN2Avi6q3qMQq1JdBvNE130_assertion wasDerivedFrom lhgdn-20090331 NP209006.RAW2M4tB5H5bNIJgAXH1wFNVaFN2Avi6q3qMQq1JdBvNE130_provenance.
- NP209006.RAW2M4tB5H5bNIJgAXH1wFNVaFN2Avi6q3qMQq1JdBvNE130_assertion SIO_000772 16912130 NP209006.RAW2M4tB5H5bNIJgAXH1wFNVaFN2Avi6q3qMQq1JdBvNE130_provenance.
- NP209006.RAW2M4tB5H5bNIJgAXH1wFNVaFN2Avi6q3qMQq1JdBvNE130_assertion evidence source_evidence_literature NP209006.RAW2M4tB5H5bNIJgAXH1wFNVaFN2Avi6q3qMQq1JdBvNE130_provenance.
- NP209006.RAW2M4tB5H5bNIJgAXH1wFNVaFN2Avi6q3qMQq1JdBvNE130_assertion description "[Three novel mutations in the GATA3 gene responsible for familial hypoparathyroidism and deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209006.RAW2M4tB5H5bNIJgAXH1wFNVaFN2Avi6q3qMQq1JdBvNE130_provenance.