Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP996643.RAFwBidKjn4ZKUqHz8UjEgFf2VnpEq4_q3-xir-qBq44g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP996643.RAFwBidKjn4ZKUqHz8UjEgFf2VnpEq4_q3-xir-qBq44g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP996643.RAFwBidKjn4ZKUqHz8UjEgFf2VnpEq4_q3-xir-qBq44g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP996643.RAFwBidKjn4ZKUqHz8UjEgFf2VnpEq4_q3-xir-qBq44g130_provenance.
- befree-2016 importedOn "2016-02-19" NP996643.RAFwBidKjn4ZKUqHz8UjEgFf2VnpEq4_q3-xir-qBq44g130_provenance.
- NP996643.RAFwBidKjn4ZKUqHz8UjEgFf2VnpEq4_q3-xir-qBq44g130_assertion wasGeneratedBy ECO_0000203 NP996643.RAFwBidKjn4ZKUqHz8UjEgFf2VnpEq4_q3-xir-qBq44g130_provenance.
- NP996643.RAFwBidKjn4ZKUqHz8UjEgFf2VnpEq4_q3-xir-qBq44g130_assertion wasDerivedFrom befree-2016 NP996643.RAFwBidKjn4ZKUqHz8UjEgFf2VnpEq4_q3-xir-qBq44g130_provenance.
- NP996643.RAFwBidKjn4ZKUqHz8UjEgFf2VnpEq4_q3-xir-qBq44g130_assertion SIO_000772 22784463 NP996643.RAFwBidKjn4ZKUqHz8UjEgFf2VnpEq4_q3-xir-qBq44g130_provenance.
- NP996643.RAFwBidKjn4ZKUqHz8UjEgFf2VnpEq4_q3-xir-qBq44g130_assertion evidence source_evidence_literature NP996643.RAFwBidKjn4ZKUqHz8UjEgFf2VnpEq4_q3-xir-qBq44g130_provenance.
- NP996643.RAFwBidKjn4ZKUqHz8UjEgFf2VnpEq4_q3-xir-qBq44g130_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." NP996643.RAFwBidKjn4ZKUqHz8UjEgFf2VnpEq4_q3-xir-qBq44g130_provenance.