Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1404986.RAXpm3NUdKO2YurNnRrBjDEv1M3rqCv9MT265xZDmJELU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1404986.RAXpm3NUdKO2YurNnRrBjDEv1M3rqCv9MT265xZDmJELU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1404986.RAXpm3NUdKO2YurNnRrBjDEv1M3rqCv9MT265xZDmJELU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1404986.RAXpm3NUdKO2YurNnRrBjDEv1M3rqCv9MT265xZDmJELU130_provenance.
- NP1404986.RAXpm3NUdKO2YurNnRrBjDEv1M3rqCv9MT265xZDmJELU130_assertion description "[We have determined the mutations and the pattern of inheritance of the XPD alleles in the 11 cases identified in Italy so far, in which the hair abnormalities diagnostic for TTD are associated with different disease severity but similar cellular photosensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1404986.RAXpm3NUdKO2YurNnRrBjDEv1M3rqCv9MT265xZDmJELU130_provenance.
- NP1404986.RAXpm3NUdKO2YurNnRrBjDEv1M3rqCv9MT265xZDmJELU130_assertion evidence source_evidence_literature NP1404986.RAXpm3NUdKO2YurNnRrBjDEv1M3rqCv9MT265xZDmJELU130_provenance.
- NP1404986.RAXpm3NUdKO2YurNnRrBjDEv1M3rqCv9MT265xZDmJELU130_assertion SIO_000772 9758621 NP1404986.RAXpm3NUdKO2YurNnRrBjDEv1M3rqCv9MT265xZDmJELU130_provenance.
- NP1404986.RAXpm3NUdKO2YurNnRrBjDEv1M3rqCv9MT265xZDmJELU130_assertion wasDerivedFrom befree-2016 NP1404986.RAXpm3NUdKO2YurNnRrBjDEv1M3rqCv9MT265xZDmJELU130_provenance.
- NP1404986.RAXpm3NUdKO2YurNnRrBjDEv1M3rqCv9MT265xZDmJELU130_assertion wasGeneratedBy ECO_0000203 NP1404986.RAXpm3NUdKO2YurNnRrBjDEv1M3rqCv9MT265xZDmJELU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1404986.RAXpm3NUdKO2YurNnRrBjDEv1M3rqCv9MT265xZDmJELU130_provenance.