Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP864480.RA_lSN-fHLHVOxXXuWPfJP8ez8o89L5BA30yoJ0364VX8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP864480.RA_lSN-fHLHVOxXXuWPfJP8ez8o89L5BA30yoJ0364VX8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP864480.RA_lSN-fHLHVOxXXuWPfJP8ez8o89L5BA30yoJ0364VX8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP864480.RA_lSN-fHLHVOxXXuWPfJP8ez8o89L5BA30yoJ0364VX8130_provenance.
- NP864480.RA_lSN-fHLHVOxXXuWPfJP8ez8o89L5BA30yoJ0364VX8130_assertion description "[CFTR and/or SPINK1 gene mutations associate with IP (idiopathic CP and IRAP) independently of the presence of PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP864480.RA_lSN-fHLHVOxXXuWPfJP8ez8o89L5BA30yoJ0364VX8130_provenance.
- NP864480.RA_lSN-fHLHVOxXXuWPfJP8ez8o89L5BA30yoJ0364VX8130_assertion evidence source_evidence_literature NP864480.RA_lSN-fHLHVOxXXuWPfJP8ez8o89L5BA30yoJ0364VX8130_provenance.
- NP864480.RA_lSN-fHLHVOxXXuWPfJP8ez8o89L5BA30yoJ0364VX8130_assertion SIO_000772 21222060 NP864480.RA_lSN-fHLHVOxXXuWPfJP8ez8o89L5BA30yoJ0364VX8130_provenance.
- NP864480.RA_lSN-fHLHVOxXXuWPfJP8ez8o89L5BA30yoJ0364VX8130_assertion wasDerivedFrom befree-2016 NP864480.RA_lSN-fHLHVOxXXuWPfJP8ez8o89L5BA30yoJ0364VX8130_provenance.
- NP864480.RA_lSN-fHLHVOxXXuWPfJP8ez8o89L5BA30yoJ0364VX8130_assertion wasGeneratedBy ECO_0000203 NP864480.RA_lSN-fHLHVOxXXuWPfJP8ez8o89L5BA30yoJ0364VX8130_provenance.
- befree-2016 importedOn "2016-02-19" NP864480.RA_lSN-fHLHVOxXXuWPfJP8ez8o89L5BA30yoJ0364VX8130_provenance.