Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP800570.RAyKbB80F5O-s669g7WWLk8cddOn-UNRo3FJeFf72UvjQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP800570.RAyKbB80F5O-s669g7WWLk8cddOn-UNRo3FJeFf72UvjQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800570.RAyKbB80F5O-s669g7WWLk8cddOn-UNRo3FJeFf72UvjQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800570.RAyKbB80F5O-s669g7WWLk8cddOn-UNRo3FJeFf72UvjQ130_provenance.
- NP800570.RAyKbB80F5O-s669g7WWLk8cddOn-UNRo3FJeFf72UvjQ130_assertion description "[As SDH mutations are virtually always germline, we conclude that approximately 15% of all pheochromocytomas or paragangliomas are associated with germline SDH mutation and that immunohistochemistry can be used to triage genetic testing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800570.RAyKbB80F5O-s669g7WWLk8cddOn-UNRo3FJeFf72UvjQ130_provenance.
- NP800570.RAyKbB80F5O-s669g7WWLk8cddOn-UNRo3FJeFf72UvjQ130_assertion evidence source_evidence_literature NP800570.RAyKbB80F5O-s669g7WWLk8cddOn-UNRo3FJeFf72UvjQ130_provenance.
- NP800570.RAyKbB80F5O-s669g7WWLk8cddOn-UNRo3FJeFf72UvjQ130_assertion SIO_000772 20236688 NP800570.RAyKbB80F5O-s669g7WWLk8cddOn-UNRo3FJeFf72UvjQ130_provenance.
- NP800570.RAyKbB80F5O-s669g7WWLk8cddOn-UNRo3FJeFf72UvjQ130_assertion wasDerivedFrom befree-2016 NP800570.RAyKbB80F5O-s669g7WWLk8cddOn-UNRo3FJeFf72UvjQ130_provenance.
- NP800570.RAyKbB80F5O-s669g7WWLk8cddOn-UNRo3FJeFf72UvjQ130_assertion wasGeneratedBy ECO_0000203 NP800570.RAyKbB80F5O-s669g7WWLk8cddOn-UNRo3FJeFf72UvjQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP800570.RAyKbB80F5O-s669g7WWLk8cddOn-UNRo3FJeFf72UvjQ130_provenance.