Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP784207.RAZz1O8VhzT0UGhCsYpWdxSiQ1DfapWZCALbpRFmkQ1Is130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP784207.RAZz1O8VhzT0UGhCsYpWdxSiQ1DfapWZCALbpRFmkQ1Is130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP784207.RAZz1O8VhzT0UGhCsYpWdxSiQ1DfapWZCALbpRFmkQ1Is130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP784207.RAZz1O8VhzT0UGhCsYpWdxSiQ1DfapWZCALbpRFmkQ1Is130_provenance.
- befree-20150227 importedOn "2015-02-27" NP784207.RAZz1O8VhzT0UGhCsYpWdxSiQ1DfapWZCALbpRFmkQ1Is130_provenance.
- NP784207.RAZz1O8VhzT0UGhCsYpWdxSiQ1DfapWZCALbpRFmkQ1Is130_assertion wasGeneratedBy ECO_0000203 NP784207.RAZz1O8VhzT0UGhCsYpWdxSiQ1DfapWZCALbpRFmkQ1Is130_provenance.
- NP784207.RAZz1O8VhzT0UGhCsYpWdxSiQ1DfapWZCALbpRFmkQ1Is130_assertion wasDerivedFrom befree-20150227 NP784207.RAZz1O8VhzT0UGhCsYpWdxSiQ1DfapWZCALbpRFmkQ1Is130_provenance.
- NP784207.RAZz1O8VhzT0UGhCsYpWdxSiQ1DfapWZCALbpRFmkQ1Is130_assertion SIO_000772 25146893 NP784207.RAZz1O8VhzT0UGhCsYpWdxSiQ1DfapWZCALbpRFmkQ1Is130_provenance.
- NP784207.RAZz1O8VhzT0UGhCsYpWdxSiQ1DfapWZCALbpRFmkQ1Is130_assertion evidence source_evidence_literature NP784207.RAZz1O8VhzT0UGhCsYpWdxSiQ1DfapWZCALbpRFmkQ1Is130_provenance.
- NP784207.RAZz1O8VhzT0UGhCsYpWdxSiQ1DfapWZCALbpRFmkQ1Is130_assertion description "[Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP784207.RAZz1O8VhzT0UGhCsYpWdxSiQ1DfapWZCALbpRFmkQ1Is130_provenance.