Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP940608.RA_VRBzLsOkcD2mMSRwiN60pztoEt0uMro7qU6_HWXkx8130_assertion> ?p ?o ?g. }
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- NP940608.RA_VRBzLsOkcD2mMSRwiN60pztoEt0uMro7qU6_HWXkx8130_assertion type Assertion NP940608.RA_VRBzLsOkcD2mMSRwiN60pztoEt0uMro7qU6_HWXkx8130_head.
- NP940608.RA_VRBzLsOkcD2mMSRwiN60pztoEt0uMro7qU6_HWXkx8130_assertion description "[Mutations in the PINK1 gene cause autosomal recessive parkinsonism characterized by early onset and a variable phenotypic presentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP940608.RA_VRBzLsOkcD2mMSRwiN60pztoEt0uMro7qU6_HWXkx8130_provenance.
- NP940608.RA_VRBzLsOkcD2mMSRwiN60pztoEt0uMro7qU6_HWXkx8130_assertion evidence source_evidence_literature NP940608.RA_VRBzLsOkcD2mMSRwiN60pztoEt0uMro7qU6_HWXkx8130_provenance.
- NP940608.RA_VRBzLsOkcD2mMSRwiN60pztoEt0uMro7qU6_HWXkx8130_assertion SIO_000772 15955954 NP940608.RA_VRBzLsOkcD2mMSRwiN60pztoEt0uMro7qU6_HWXkx8130_provenance.
- NP940608.RA_VRBzLsOkcD2mMSRwiN60pztoEt0uMro7qU6_HWXkx8130_assertion wasDerivedFrom befree-20150227 NP940608.RA_VRBzLsOkcD2mMSRwiN60pztoEt0uMro7qU6_HWXkx8130_provenance.
- NP940608.RA_VRBzLsOkcD2mMSRwiN60pztoEt0uMro7qU6_HWXkx8130_assertion wasGeneratedBy ECO_0000203 NP940608.RA_VRBzLsOkcD2mMSRwiN60pztoEt0uMro7qU6_HWXkx8130_provenance.