Matches in Nanopublications for { ?s ?p "[Two variants, 1672C>T in SLC22A4 and -207G>C in SLC22A5, were shown to alter these genes' functions and were identified as genetic susceptibility factors for Crohn's disease (CD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP51659.RAgPFn-AAFzVn-ZVVzuOpRbrfStzgKUVYDRQoLqgRng58130_assertion description "[Two variants, 1672C>T in SLC22A4 and -207G>C in SLC22A5, were shown to alter these genes' functions and were identified as genetic susceptibility factors for Crohn's disease (CD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51659.RAgPFn-AAFzVn-ZVVzuOpRbrfStzgKUVYDRQoLqgRng58130_provenance.
- NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_assertion description "[Two variants, 1672C>T in SLC22A4 and -207G>C in SLC22A5, were shown to alter these genes' functions and were identified as genetic susceptibility factors for Crohn's disease (CD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_provenance.
- assertion description "[Two variants, 1672C>T in SLC22A4 and -207G>C in SLC22A5, were shown to alter these genes' functions and were identified as genetic susceptibility factors for Crohn's disease (CD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Two variants, 1672C>T in SLC22A4 and -207G>C in SLC22A5, were shown to alter these genes' functions and were identified as genetic susceptibility factors for Crohn's disease (CD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP97645.RAUS5So2-yB49fROTMx0aV1fLPSVYO5GQE22n648iPAdc130_assertion description "[Two variants, 1672C>T in SLC22A4 and -207G>C in SLC22A5, were shown to alter these genes' functions and were identified as genetic susceptibility factors for Crohn's disease (CD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP97645.RAUS5So2-yB49fROTMx0aV1fLPSVYO5GQE22n648iPAdc130_provenance.
- NP97646.RAmVuC7prjFiA3oomw-9XftyicXWYFlL70KnuResOVRac130_assertion description "[Two variants, 1672C>T in SLC22A4 and -207G>C in SLC22A5, were shown to alter these genes' functions and were identified as genetic susceptibility factors for Crohn's disease (CD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP97646.RAmVuC7prjFiA3oomw-9XftyicXWYFlL70KnuResOVRac130_provenance.