Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP730752.RAUl-2Z716vTOzj2cbG0hVLok9C_R9S46YnO9F7gmQpRM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP730752.RAUl-2Z716vTOzj2cbG0hVLok9C_R9S46YnO9F7gmQpRM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP730752.RAUl-2Z716vTOzj2cbG0hVLok9C_R9S46YnO9F7gmQpRM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP730752.RAUl-2Z716vTOzj2cbG0hVLok9C_R9S46YnO9F7gmQpRM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP730752.RAUl-2Z716vTOzj2cbG0hVLok9C_R9S46YnO9F7gmQpRM130_provenance.
- NP730752.RAUl-2Z716vTOzj2cbG0hVLok9C_R9S46YnO9F7gmQpRM130_assertion wasGeneratedBy ECO_0000203 NP730752.RAUl-2Z716vTOzj2cbG0hVLok9C_R9S46YnO9F7gmQpRM130_provenance.
- NP730752.RAUl-2Z716vTOzj2cbG0hVLok9C_R9S46YnO9F7gmQpRM130_assertion wasDerivedFrom befree-20150227 NP730752.RAUl-2Z716vTOzj2cbG0hVLok9C_R9S46YnO9F7gmQpRM130_provenance.
- NP730752.RAUl-2Z716vTOzj2cbG0hVLok9C_R9S46YnO9F7gmQpRM130_assertion SIO_000772 22784463 NP730752.RAUl-2Z716vTOzj2cbG0hVLok9C_R9S46YnO9F7gmQpRM130_provenance.
- NP730752.RAUl-2Z716vTOzj2cbG0hVLok9C_R9S46YnO9F7gmQpRM130_assertion evidence source_evidence_literature NP730752.RAUl-2Z716vTOzj2cbG0hVLok9C_R9S46YnO9F7gmQpRM130_provenance.
- NP730752.RAUl-2Z716vTOzj2cbG0hVLok9C_R9S46YnO9F7gmQpRM130_assertion description "[Clinical and genetic analysis of a compound heterozygous mutation in the thyroglobulin gene in a Chinese twin family with congenital goiter and hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP730752.RAUl-2Z716vTOzj2cbG0hVLok9C_R9S46YnO9F7gmQpRM130_provenance.