Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP746283.RAAfGSOIxho_tnQu-ntpNLeDlgPwkM30gIfvYrNws9GfQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP746283.RAAfGSOIxho_tnQu-ntpNLeDlgPwkM30gIfvYrNws9GfQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP746283.RAAfGSOIxho_tnQu-ntpNLeDlgPwkM30gIfvYrNws9GfQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP746283.RAAfGSOIxho_tnQu-ntpNLeDlgPwkM30gIfvYrNws9GfQ130_provenance.
- NP746283.RAAfGSOIxho_tnQu-ntpNLeDlgPwkM30gIfvYrNws9GfQ130_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." NP746283.RAAfGSOIxho_tnQu-ntpNLeDlgPwkM30gIfvYrNws9GfQ130_provenance.
- NP746283.RAAfGSOIxho_tnQu-ntpNLeDlgPwkM30gIfvYrNws9GfQ130_assertion evidence source_evidence_literature NP746283.RAAfGSOIxho_tnQu-ntpNLeDlgPwkM30gIfvYrNws9GfQ130_provenance.
- NP746283.RAAfGSOIxho_tnQu-ntpNLeDlgPwkM30gIfvYrNws9GfQ130_assertion SIO_000772 21222060 NP746283.RAAfGSOIxho_tnQu-ntpNLeDlgPwkM30gIfvYrNws9GfQ130_provenance.
- NP746283.RAAfGSOIxho_tnQu-ntpNLeDlgPwkM30gIfvYrNws9GfQ130_assertion wasDerivedFrom befree-20140225 NP746283.RAAfGSOIxho_tnQu-ntpNLeDlgPwkM30gIfvYrNws9GfQ130_provenance.
- NP746283.RAAfGSOIxho_tnQu-ntpNLeDlgPwkM30gIfvYrNws9GfQ130_assertion wasGeneratedBy ECO_0000203 NP746283.RAAfGSOIxho_tnQu-ntpNLeDlgPwkM30gIfvYrNws9GfQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP746283.RAAfGSOIxho_tnQu-ntpNLeDlgPwkM30gIfvYrNws9GfQ130_provenance.