Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1231316.RAX9Oe3MVPA9vTa47LhPzrL2JADPh6bqoaNY6Jv8JyHsI130_assertion> ?p ?o ?g. }
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- NP1231316.RAX9Oe3MVPA9vTa47LhPzrL2JADPh6bqoaNY6Jv8JyHsI130_assertion type Assertion NP1231316.RAX9Oe3MVPA9vTa47LhPzrL2JADPh6bqoaNY6Jv8JyHsI130_head.
- NP1231316.RAX9Oe3MVPA9vTa47LhPzrL2JADPh6bqoaNY6Jv8JyHsI130_assertion description "[The HDAC4 (2q37.2) variant rs73000144 (OR = 14.6, p = 0.018) and the EFCAB13 (17q21.3) variant rs118004742 (OR = 1.8, p = 0.048) were overrepresented in patients with familial PrCa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1231316.RAX9Oe3MVPA9vTa47LhPzrL2JADPh6bqoaNY6Jv8JyHsI130_provenance.
- NP1231316.RAX9Oe3MVPA9vTa47LhPzrL2JADPh6bqoaNY6Jv8JyHsI130_assertion evidence source_evidence_literature NP1231316.RAX9Oe3MVPA9vTa47LhPzrL2JADPh6bqoaNY6Jv8JyHsI130_provenance.
- NP1231316.RAX9Oe3MVPA9vTa47LhPzrL2JADPh6bqoaNY6Jv8JyHsI130_assertion SIO_000772 25335771 NP1231316.RAX9Oe3MVPA9vTa47LhPzrL2JADPh6bqoaNY6Jv8JyHsI130_provenance.
- NP1231316.RAX9Oe3MVPA9vTa47LhPzrL2JADPh6bqoaNY6Jv8JyHsI130_assertion wasDerivedFrom befree-2016 NP1231316.RAX9Oe3MVPA9vTa47LhPzrL2JADPh6bqoaNY6Jv8JyHsI130_provenance.
- NP1231316.RAX9Oe3MVPA9vTa47LhPzrL2JADPh6bqoaNY6Jv8JyHsI130_assertion wasGeneratedBy ECO_0000203 NP1231316.RAX9Oe3MVPA9vTa47LhPzrL2JADPh6bqoaNY6Jv8JyHsI130_provenance.