Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP503570.RAAOV49hjUelTm-E3pNLQs9Ugn55NbcKocpFnBO6sEJOo130_assertion> ?p ?o ?g. }
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- NP503570.RAAOV49hjUelTm-E3pNLQs9Ugn55NbcKocpFnBO6sEJOo130_assertion type Assertion NP503570.RAAOV49hjUelTm-E3pNLQs9Ugn55NbcKocpFnBO6sEJOo130_head.
- NP503570.RAAOV49hjUelTm-E3pNLQs9Ugn55NbcKocpFnBO6sEJOo130_assertion wasGeneratedBy ECO_0000203 NP503570.RAAOV49hjUelTm-E3pNLQs9Ugn55NbcKocpFnBO6sEJOo130_provenance.
- NP503570.RAAOV49hjUelTm-E3pNLQs9Ugn55NbcKocpFnBO6sEJOo130_assertion wasDerivedFrom befree-20140225 NP503570.RAAOV49hjUelTm-E3pNLQs9Ugn55NbcKocpFnBO6sEJOo130_provenance.
- NP503570.RAAOV49hjUelTm-E3pNLQs9Ugn55NbcKocpFnBO6sEJOo130_assertion SIO_000772 15007723 NP503570.RAAOV49hjUelTm-E3pNLQs9Ugn55NbcKocpFnBO6sEJOo130_provenance.
- NP503570.RAAOV49hjUelTm-E3pNLQs9Ugn55NbcKocpFnBO6sEJOo130_assertion evidence source_evidence_literature NP503570.RAAOV49hjUelTm-E3pNLQs9Ugn55NbcKocpFnBO6sEJOo130_provenance.
- NP503570.RAAOV49hjUelTm-E3pNLQs9Ugn55NbcKocpFnBO6sEJOo130_assertion description "[A TSC2-PKD1 contiguous gene syndrome caused by chromosomal microdeletions disrupting both the TSC2 and PKD1 genes has been identified in patients with TSC and early-onset severe ADPKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503570.RAAOV49hjUelTm-E3pNLQs9Ugn55NbcKocpFnBO6sEJOo130_provenance.