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- NP864478.RAAkc7TJGE5LXi1PR7P2pk_oVe2fMvl511YHORBG40dNs130_assertion type Assertion NP864478.RAAkc7TJGE5LXi1PR7P2pk_oVe2fMvl511YHORBG40dNs130_head.
- NP864478.RAAkc7TJGE5LXi1PR7P2pk_oVe2fMvl511YHORBG40dNs130_assertion wasGeneratedBy ECO_0000203 NP864478.RAAkc7TJGE5LXi1PR7P2pk_oVe2fMvl511YHORBG40dNs130_provenance.
- NP864478.RAAkc7TJGE5LXi1PR7P2pk_oVe2fMvl511YHORBG40dNs130_assertion wasDerivedFrom befree-2016 NP864478.RAAkc7TJGE5LXi1PR7P2pk_oVe2fMvl511YHORBG40dNs130_provenance.
- NP864478.RAAkc7TJGE5LXi1PR7P2pk_oVe2fMvl511YHORBG40dNs130_assertion SIO_000772 21222060 NP864478.RAAkc7TJGE5LXi1PR7P2pk_oVe2fMvl511YHORBG40dNs130_provenance.
- NP864478.RAAkc7TJGE5LXi1PR7P2pk_oVe2fMvl511YHORBG40dNs130_assertion evidence source_evidence_literature NP864478.RAAkc7TJGE5LXi1PR7P2pk_oVe2fMvl511YHORBG40dNs130_provenance.
- NP864478.RAAkc7TJGE5LXi1PR7P2pk_oVe2fMvl511YHORBG40dNs130_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." NP864478.RAAkc7TJGE5LXi1PR7P2pk_oVe2fMvl511YHORBG40dNs130_provenance.