Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP197325.RACD6Fmv6-PL-T3aAjL_PglsOKz_urVf3IQIKVsW5irL8130_assertion> ?p ?o ?g. }
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- NP197325.RACD6Fmv6-PL-T3aAjL_PglsOKz_urVf3IQIKVsW5irL8130_assertion type Assertion NP197325.RACD6Fmv6-PL-T3aAjL_PglsOKz_urVf3IQIKVsW5irL8130_head.
- NP197325.RACD6Fmv6-PL-T3aAjL_PglsOKz_urVf3IQIKVsW5irL8130_assertion description "[Mutations in the PINK1 gene are the second most common cause after parkin of autosomal recessive early-onset Parkinson's disease (PD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP197325.RACD6Fmv6-PL-T3aAjL_PglsOKz_urVf3IQIKVsW5irL8130_provenance.
- NP197325.RACD6Fmv6-PL-T3aAjL_PglsOKz_urVf3IQIKVsW5irL8130_assertion evidence source_evidence_literature NP197325.RACD6Fmv6-PL-T3aAjL_PglsOKz_urVf3IQIKVsW5irL8130_provenance.
- NP197325.RACD6Fmv6-PL-T3aAjL_PglsOKz_urVf3IQIKVsW5irL8130_assertion SIO_000772 20558144 NP197325.RACD6Fmv6-PL-T3aAjL_PglsOKz_urVf3IQIKVsW5irL8130_provenance.
- NP197325.RACD6Fmv6-PL-T3aAjL_PglsOKz_urVf3IQIKVsW5irL8130_assertion wasDerivedFrom befree-20140225 NP197325.RACD6Fmv6-PL-T3aAjL_PglsOKz_urVf3IQIKVsW5irL8130_provenance.
- NP197325.RACD6Fmv6-PL-T3aAjL_PglsOKz_urVf3IQIKVsW5irL8130_assertion wasGeneratedBy ECO_0000203 NP197325.RACD6Fmv6-PL-T3aAjL_PglsOKz_urVf3IQIKVsW5irL8130_provenance.