Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP205894.RAzMz2rRowKNaPm6KofY08H6CEWWxpV3iCeAw1dkdzcm4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP205894.RAzMz2rRowKNaPm6KofY08H6CEWWxpV3iCeAw1dkdzcm4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP205894.RAzMz2rRowKNaPm6KofY08H6CEWWxpV3iCeAw1dkdzcm4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP205894.RAzMz2rRowKNaPm6KofY08H6CEWWxpV3iCeAw1dkdzcm4130_provenance.
- NP205894.RAzMz2rRowKNaPm6KofY08H6CEWWxpV3iCeAw1dkdzcm4130_assertion wasGeneratedBy ECO_0000203 NP205894.RAzMz2rRowKNaPm6KofY08H6CEWWxpV3iCeAw1dkdzcm4130_provenance.
- NP205894.RAzMz2rRowKNaPm6KofY08H6CEWWxpV3iCeAw1dkdzcm4130_assertion wasDerivedFrom befree-20140225 NP205894.RAzMz2rRowKNaPm6KofY08H6CEWWxpV3iCeAw1dkdzcm4130_provenance.
- NP205894.RAzMz2rRowKNaPm6KofY08H6CEWWxpV3iCeAw1dkdzcm4130_assertion SIO_000772 16092045 NP205894.RAzMz2rRowKNaPm6KofY08H6CEWWxpV3iCeAw1dkdzcm4130_provenance.
- NP205894.RAzMz2rRowKNaPm6KofY08H6CEWWxpV3iCeAw1dkdzcm4130_assertion evidence source_evidence_literature NP205894.RAzMz2rRowKNaPm6KofY08H6CEWWxpV3iCeAw1dkdzcm4130_provenance.
- NP205894.RAzMz2rRowKNaPm6KofY08H6CEWWxpV3iCeAw1dkdzcm4130_assertion description "[In an extended family (Italy-6) of 46 members with clinical phenotypes of gestational diabetes, MODY, and T2D, a single nucleotide change of CCT to ACT was identified at codon 33 resulting in a Pro to Thr substitution (P33T) in the IPF1 transactivation domain that also contributes to an altered metabolic status in the unaffected NM subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205894.RAzMz2rRowKNaPm6KofY08H6CEWWxpV3iCeAw1dkdzcm4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP205894.RAzMz2rRowKNaPm6KofY08H6CEWWxpV3iCeAw1dkdzcm4130_provenance.