Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP126843.RA5TUqJwpcOB7R3h9hU8lc1whsxCT_6S3fldlnvV8Waik130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP126843.RA5TUqJwpcOB7R3h9hU8lc1whsxCT_6S3fldlnvV8Waik130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP126843.RA5TUqJwpcOB7R3h9hU8lc1whsxCT_6S3fldlnvV8Waik130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP126843.RA5TUqJwpcOB7R3h9hU8lc1whsxCT_6S3fldlnvV8Waik130_provenance.
- NP126843.RA5TUqJwpcOB7R3h9hU8lc1whsxCT_6S3fldlnvV8Waik130_assertion description "[Disorders caused by mutations in the ARX gene include: hydrocephaly, lissencephaly and agenesis of corpus callosum with abnormal genitalia, Partington syndrome S), X-linked infantile spasms, myoclonic epilepsy, and nonspecific mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP126843.RA5TUqJwpcOB7R3h9hU8lc1whsxCT_6S3fldlnvV8Waik130_provenance.
- NP126843.RA5TUqJwpcOB7R3h9hU8lc1whsxCT_6S3fldlnvV8Waik130_assertion evidence source_evidence_literature NP126843.RA5TUqJwpcOB7R3h9hU8lc1whsxCT_6S3fldlnvV8Waik130_provenance.
- NP126843.RA5TUqJwpcOB7R3h9hU8lc1whsxCT_6S3fldlnvV8Waik130_assertion SIO_000772 18975239 NP126843.RA5TUqJwpcOB7R3h9hU8lc1whsxCT_6S3fldlnvV8Waik130_provenance.
- NP126843.RA5TUqJwpcOB7R3h9hU8lc1whsxCT_6S3fldlnvV8Waik130_assertion wasDerivedFrom lhgdn-20090331 NP126843.RA5TUqJwpcOB7R3h9hU8lc1whsxCT_6S3fldlnvV8Waik130_provenance.
- NP126843.RA5TUqJwpcOB7R3h9hU8lc1whsxCT_6S3fldlnvV8Waik130_assertion wasGeneratedBy ECO_0000203 NP126843.RA5TUqJwpcOB7R3h9hU8lc1whsxCT_6S3fldlnvV8Waik130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP126843.RA5TUqJwpcOB7R3h9hU8lc1whsxCT_6S3fldlnvV8Waik130_provenance.