Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP738759.RA08B9JLC-AnILtW9NG6LZbW6-IAQbEv8ka7Edx-NbAfM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP738759.RA08B9JLC-AnILtW9NG6LZbW6-IAQbEv8ka7Edx-NbAfM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP738759.RA08B9JLC-AnILtW9NG6LZbW6-IAQbEv8ka7Edx-NbAfM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP738759.RA08B9JLC-AnILtW9NG6LZbW6-IAQbEv8ka7Edx-NbAfM130_provenance.
- NP738759.RA08B9JLC-AnILtW9NG6LZbW6-IAQbEv8ka7Edx-NbAfM130_assertion description "[In conclusion we describe the first Italian case of congenital hypothyroidism due to a new deletion in the NIS gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP738759.RA08B9JLC-AnILtW9NG6LZbW6-IAQbEv8ka7Edx-NbAfM130_provenance.
- NP738759.RA08B9JLC-AnILtW9NG6LZbW6-IAQbEv8ka7Edx-NbAfM130_assertion evidence source_evidence_literature NP738759.RA08B9JLC-AnILtW9NG6LZbW6-IAQbEv8ka7Edx-NbAfM130_provenance.
- NP738759.RA08B9JLC-AnILtW9NG6LZbW6-IAQbEv8ka7Edx-NbAfM130_assertion SIO_000772 14510914 NP738759.RA08B9JLC-AnILtW9NG6LZbW6-IAQbEv8ka7Edx-NbAfM130_provenance.
- NP738759.RA08B9JLC-AnILtW9NG6LZbW6-IAQbEv8ka7Edx-NbAfM130_assertion wasDerivedFrom befree-20140225 NP738759.RA08B9JLC-AnILtW9NG6LZbW6-IAQbEv8ka7Edx-NbAfM130_provenance.
- NP738759.RA08B9JLC-AnILtW9NG6LZbW6-IAQbEv8ka7Edx-NbAfM130_assertion wasGeneratedBy ECO_0000203 NP738759.RA08B9JLC-AnILtW9NG6LZbW6-IAQbEv8ka7Edx-NbAfM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP738759.RA08B9JLC-AnILtW9NG6LZbW6-IAQbEv8ka7Edx-NbAfM130_provenance.