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- source_evidence_literature type ECO_0000212 NP174514.RA_XFAZtwwteKbv63Z21zxjtCRNWzgH9ReEyIxaM8dwwo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP174514.RA_XFAZtwwteKbv63Z21zxjtCRNWzgH9ReEyIxaM8dwwo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP174514.RA_XFAZtwwteKbv63Z21zxjtCRNWzgH9ReEyIxaM8dwwo130_provenance.
- NP174514.RA_XFAZtwwteKbv63Z21zxjtCRNWzgH9ReEyIxaM8dwwo130_assertion description "[The lamin A/C (LMNA) gene, mutations of which cause rare syndromes of severe insulin resistance and dyslipidemia, is located on chromosome 1q21-q24, a region linked to T2DM in several genome wide scans, including in the Old Order Amish.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP174514.RA_XFAZtwwteKbv63Z21zxjtCRNWzgH9ReEyIxaM8dwwo130_provenance.
- NP174514.RA_XFAZtwwteKbv63Z21zxjtCRNWzgH9ReEyIxaM8dwwo130_assertion evidence source_evidence_literature NP174514.RA_XFAZtwwteKbv63Z21zxjtCRNWzgH9ReEyIxaM8dwwo130_provenance.
- NP174514.RA_XFAZtwwteKbv63Z21zxjtCRNWzgH9ReEyIxaM8dwwo130_assertion SIO_000772 15205219 NP174514.RA_XFAZtwwteKbv63Z21zxjtCRNWzgH9ReEyIxaM8dwwo130_provenance.
- NP174514.RA_XFAZtwwteKbv63Z21zxjtCRNWzgH9ReEyIxaM8dwwo130_assertion wasDerivedFrom befree-20140225 NP174514.RA_XFAZtwwteKbv63Z21zxjtCRNWzgH9ReEyIxaM8dwwo130_provenance.
- NP174514.RA_XFAZtwwteKbv63Z21zxjtCRNWzgH9ReEyIxaM8dwwo130_assertion wasGeneratedBy ECO_0000203 NP174514.RA_XFAZtwwteKbv63Z21zxjtCRNWzgH9ReEyIxaM8dwwo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP174514.RA_XFAZtwwteKbv63Z21zxjtCRNWzgH9ReEyIxaM8dwwo130_provenance.