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- source_evidence_literature type ECO_0000212 NP583273.RAe6s3R1vssPK0rnH7DhNnvbhK3-fu7nC2CxT2pgLgWY4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583273.RAe6s3R1vssPK0rnH7DhNnvbhK3-fu7nC2CxT2pgLgWY4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583273.RAe6s3R1vssPK0rnH7DhNnvbhK3-fu7nC2CxT2pgLgWY4130_provenance.
- NP583273.RAe6s3R1vssPK0rnH7DhNnvbhK3-fu7nC2CxT2pgLgWY4130_assertion description "[Novel mutations in the Atlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to the SPG3A locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583273.RAe6s3R1vssPK0rnH7DhNnvbhK3-fu7nC2CxT2pgLgWY4130_provenance.
- NP583273.RAe6s3R1vssPK0rnH7DhNnvbhK3-fu7nC2CxT2pgLgWY4130_assertion evidence source_evidence_literature NP583273.RAe6s3R1vssPK0rnH7DhNnvbhK3-fu7nC2CxT2pgLgWY4130_provenance.
- NP583273.RAe6s3R1vssPK0rnH7DhNnvbhK3-fu7nC2CxT2pgLgWY4130_assertion SIO_000772 14695538 NP583273.RAe6s3R1vssPK0rnH7DhNnvbhK3-fu7nC2CxT2pgLgWY4130_provenance.
- NP583273.RAe6s3R1vssPK0rnH7DhNnvbhK3-fu7nC2CxT2pgLgWY4130_assertion wasDerivedFrom befree-20140225 NP583273.RAe6s3R1vssPK0rnH7DhNnvbhK3-fu7nC2CxT2pgLgWY4130_provenance.
- NP583273.RAe6s3R1vssPK0rnH7DhNnvbhK3-fu7nC2CxT2pgLgWY4130_assertion wasGeneratedBy ECO_0000203 NP583273.RAe6s3R1vssPK0rnH7DhNnvbhK3-fu7nC2CxT2pgLgWY4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP583273.RAe6s3R1vssPK0rnH7DhNnvbhK3-fu7nC2CxT2pgLgWY4130_provenance.