Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP400922.RA3rgyCPw1c7vIlNK6GgcGFM-w7yyyN1Kcy1hmsXWBdj0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP400922.RA3rgyCPw1c7vIlNK6GgcGFM-w7yyyN1Kcy1hmsXWBdj0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400922.RA3rgyCPw1c7vIlNK6GgcGFM-w7yyyN1Kcy1hmsXWBdj0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400922.RA3rgyCPw1c7vIlNK6GgcGFM-w7yyyN1Kcy1hmsXWBdj0130_provenance.
- NP400922.RA3rgyCPw1c7vIlNK6GgcGFM-w7yyyN1Kcy1hmsXWBdj0130_assertion description "[We dichotomized the whole cohort based on the presence or absence of N34S SPINK1 and L26V CTSB mutations and further subdivided them into TCP and FCPD patients and compared the distribution of TCF7L2 variants between them.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400922.RA3rgyCPw1c7vIlNK6GgcGFM-w7yyyN1Kcy1hmsXWBdj0130_provenance.
- NP400922.RA3rgyCPw1c7vIlNK6GgcGFM-w7yyyN1Kcy1hmsXWBdj0130_assertion evidence source_evidence_literature NP400922.RA3rgyCPw1c7vIlNK6GgcGFM-w7yyyN1Kcy1hmsXWBdj0130_provenance.
- NP400922.RA3rgyCPw1c7vIlNK6GgcGFM-w7yyyN1Kcy1hmsXWBdj0130_assertion SIO_000772 18706099 NP400922.RA3rgyCPw1c7vIlNK6GgcGFM-w7yyyN1Kcy1hmsXWBdj0130_provenance.
- NP400922.RA3rgyCPw1c7vIlNK6GgcGFM-w7yyyN1Kcy1hmsXWBdj0130_assertion wasDerivedFrom befree-20140225 NP400922.RA3rgyCPw1c7vIlNK6GgcGFM-w7yyyN1Kcy1hmsXWBdj0130_provenance.
- NP400922.RA3rgyCPw1c7vIlNK6GgcGFM-w7yyyN1Kcy1hmsXWBdj0130_assertion wasGeneratedBy ECO_0000203 NP400922.RA3rgyCPw1c7vIlNK6GgcGFM-w7yyyN1Kcy1hmsXWBdj0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP400922.RA3rgyCPw1c7vIlNK6GgcGFM-w7yyyN1Kcy1hmsXWBdj0130_provenance.