Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP896016.RA_lMVUnZ5VS3GirCRS2O1hwtYU8qstbN0mdhUCSwyujw130_assertion> ?p ?o ?g. }
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- NP896016.RA_lMVUnZ5VS3GirCRS2O1hwtYU8qstbN0mdhUCSwyujw130_assertion type Assertion NP896016.RA_lMVUnZ5VS3GirCRS2O1hwtYU8qstbN0mdhUCSwyujw130_head.
- NP896016.RA_lMVUnZ5VS3GirCRS2O1hwtYU8qstbN0mdhUCSwyujw130_assertion description "[We then screened 200 T2D siblings/families for PSMD9 +nt460A/G, +nt437C/T and exon E197G A/G single nucleotide polymorphisms (SNPs) and performed a non-parametric linkage study to test for linkage for coronary artery disease, stroke/TIA, macro-vasculopathy and macrovascular pathology of T2D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP896016.RA_lMVUnZ5VS3GirCRS2O1hwtYU8qstbN0mdhUCSwyujw130_provenance.
- NP896016.RA_lMVUnZ5VS3GirCRS2O1hwtYU8qstbN0mdhUCSwyujw130_assertion evidence source_evidence_literature NP896016.RA_lMVUnZ5VS3GirCRS2O1hwtYU8qstbN0mdhUCSwyujw130_provenance.
- NP896016.RA_lMVUnZ5VS3GirCRS2O1hwtYU8qstbN0mdhUCSwyujw130_assertion SIO_000772 21496327 NP896016.RA_lMVUnZ5VS3GirCRS2O1hwtYU8qstbN0mdhUCSwyujw130_provenance.
- NP896016.RA_lMVUnZ5VS3GirCRS2O1hwtYU8qstbN0mdhUCSwyujw130_assertion wasDerivedFrom befree-20140225 NP896016.RA_lMVUnZ5VS3GirCRS2O1hwtYU8qstbN0mdhUCSwyujw130_provenance.
- NP896016.RA_lMVUnZ5VS3GirCRS2O1hwtYU8qstbN0mdhUCSwyujw130_assertion wasGeneratedBy ECO_0000203 NP896016.RA_lMVUnZ5VS3GirCRS2O1hwtYU8qstbN0mdhUCSwyujw130_provenance.