Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP302515.RAJLzWBQLPY8rOXM8KhgC8Qg9HCP2fAfXndUMASiCbITg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP302515.RAJLzWBQLPY8rOXM8KhgC8Qg9HCP2fAfXndUMASiCbITg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP302515.RAJLzWBQLPY8rOXM8KhgC8Qg9HCP2fAfXndUMASiCbITg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP302515.RAJLzWBQLPY8rOXM8KhgC8Qg9HCP2fAfXndUMASiCbITg130_provenance.
- NP302515.RAJLzWBQLPY8rOXM8KhgC8Qg9HCP2fAfXndUMASiCbITg130_assertion description "[In conclusion, the identification of different molecular defects provided evidence that hereditary goiter associated with abnormal Tg or TPO synthesis is caused by heterogeneous genetic alterations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP302515.RAJLzWBQLPY8rOXM8KhgC8Qg9HCP2fAfXndUMASiCbITg130_provenance.
- NP302515.RAJLzWBQLPY8rOXM8KhgC8Qg9HCP2fAfXndUMASiCbITg130_assertion evidence source_evidence_literature NP302515.RAJLzWBQLPY8rOXM8KhgC8Qg9HCP2fAfXndUMASiCbITg130_provenance.
- NP302515.RAJLzWBQLPY8rOXM8KhgC8Qg9HCP2fAfXndUMASiCbITg130_assertion SIO_000772 7549998 NP302515.RAJLzWBQLPY8rOXM8KhgC8Qg9HCP2fAfXndUMASiCbITg130_provenance.
- NP302515.RAJLzWBQLPY8rOXM8KhgC8Qg9HCP2fAfXndUMASiCbITg130_assertion wasDerivedFrom befree-20140225 NP302515.RAJLzWBQLPY8rOXM8KhgC8Qg9HCP2fAfXndUMASiCbITg130_provenance.
- NP302515.RAJLzWBQLPY8rOXM8KhgC8Qg9HCP2fAfXndUMASiCbITg130_assertion wasGeneratedBy ECO_0000203 NP302515.RAJLzWBQLPY8rOXM8KhgC8Qg9HCP2fAfXndUMASiCbITg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP302515.RAJLzWBQLPY8rOXM8KhgC8Qg9HCP2fAfXndUMASiCbITg130_provenance.