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- source_evidence_literature type ECO_0000212 NP308946.RA32bQ0djTIw_aUhe8Af4r_Zog_Re7mPd72XKRUc5freE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP308946.RA32bQ0djTIw_aUhe8Af4r_Zog_Re7mPd72XKRUc5freE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP308946.RA32bQ0djTIw_aUhe8Af4r_Zog_Re7mPd72XKRUc5freE130_provenance.
- NP308946.RA32bQ0djTIw_aUhe8Af4r_Zog_Re7mPd72XKRUc5freE130_assertion description "[This mutation is equivalent to the 102L mutation in the human PrP gene which is associated with Gerstmann-Str�ussler syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP308946.RA32bQ0djTIw_aUhe8Af4r_Zog_Re7mPd72XKRUc5freE130_provenance.
- NP308946.RA32bQ0djTIw_aUhe8Af4r_Zog_Re7mPd72XKRUc5freE130_assertion evidence source_evidence_literature NP308946.RA32bQ0djTIw_aUhe8Af4r_Zog_Re7mPd72XKRUc5freE130_provenance.
- NP308946.RA32bQ0djTIw_aUhe8Af4r_Zog_Re7mPd72XKRUc5freE130_assertion SIO_000772 11214938 NP308946.RA32bQ0djTIw_aUhe8Af4r_Zog_Re7mPd72XKRUc5freE130_provenance.
- NP308946.RA32bQ0djTIw_aUhe8Af4r_Zog_Re7mPd72XKRUc5freE130_assertion wasDerivedFrom befree-2016 NP308946.RA32bQ0djTIw_aUhe8Af4r_Zog_Re7mPd72XKRUc5freE130_provenance.
- NP308946.RA32bQ0djTIw_aUhe8Af4r_Zog_Re7mPd72XKRUc5freE130_assertion wasGeneratedBy ECO_0000203 NP308946.RA32bQ0djTIw_aUhe8Af4r_Zog_Re7mPd72XKRUc5freE130_provenance.
- befree-2016 importedOn "2016-02-19" NP308946.RA32bQ0djTIw_aUhe8Af4r_Zog_Re7mPd72XKRUc5freE130_provenance.