Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP356644.RAjo0if0QdWck0yKRrPjuLdMCDvkPv-c2Xcy0J-s6SAWc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP356644.RAjo0if0QdWck0yKRrPjuLdMCDvkPv-c2Xcy0J-s6SAWc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP356644.RAjo0if0QdWck0yKRrPjuLdMCDvkPv-c2Xcy0J-s6SAWc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP356644.RAjo0if0QdWck0yKRrPjuLdMCDvkPv-c2Xcy0J-s6SAWc130_provenance.
- NP356644.RAjo0if0QdWck0yKRrPjuLdMCDvkPv-c2Xcy0J-s6SAWc130_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." NP356644.RAjo0if0QdWck0yKRrPjuLdMCDvkPv-c2Xcy0J-s6SAWc130_provenance.
- NP356644.RAjo0if0QdWck0yKRrPjuLdMCDvkPv-c2Xcy0J-s6SAWc130_assertion evidence source_evidence_literature NP356644.RAjo0if0QdWck0yKRrPjuLdMCDvkPv-c2Xcy0J-s6SAWc130_provenance.
- NP356644.RAjo0if0QdWck0yKRrPjuLdMCDvkPv-c2Xcy0J-s6SAWc130_assertion SIO_000772 15955954 NP356644.RAjo0if0QdWck0yKRrPjuLdMCDvkPv-c2Xcy0J-s6SAWc130_provenance.
- NP356644.RAjo0if0QdWck0yKRrPjuLdMCDvkPv-c2Xcy0J-s6SAWc130_assertion wasDerivedFrom befree-20140225 NP356644.RAjo0if0QdWck0yKRrPjuLdMCDvkPv-c2Xcy0J-s6SAWc130_provenance.
- NP356644.RAjo0if0QdWck0yKRrPjuLdMCDvkPv-c2Xcy0J-s6SAWc130_assertion wasGeneratedBy ECO_0000203 NP356644.RAjo0if0QdWck0yKRrPjuLdMCDvkPv-c2Xcy0J-s6SAWc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP356644.RAjo0if0QdWck0yKRrPjuLdMCDvkPv-c2Xcy0J-s6SAWc130_provenance.