Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP746283.RAAfGSOIxho_tnQu-ntpNLeDlgPwkM30gIfvYrNws9GfQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP746283.RAAfGSOIxho_tnQu-ntpNLeDlgPwkM30gIfvYrNws9GfQ130_assertion type Assertion NP746283.RAAfGSOIxho_tnQu-ntpNLeDlgPwkM30gIfvYrNws9GfQ130_head.
- 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.