Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_assertion type Assertion NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_head.
- NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_assertion wasGeneratedBy ECO_0000203 NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_provenance.
- NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_assertion wasDerivedFrom befree-2016 NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_provenance.
- NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_assertion SIO_000772 17914928 NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_provenance.
- NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_assertion evidence source_evidence_literature NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_provenance.
- NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_assertion description "[Genetic linkage analysis and mutation studies have identified CYP1B1 as a causative gene in PCG, as a modifier gene in POAG, and, on rare occasions, as causative gene in POAG as well as in several ASD disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_provenance.