Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP825221.RAYWur2yetCqRcDljUlZvEvcS3c1TL2XVIXNdicA-nYzs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP825221.RAYWur2yetCqRcDljUlZvEvcS3c1TL2XVIXNdicA-nYzs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP825221.RAYWur2yetCqRcDljUlZvEvcS3c1TL2XVIXNdicA-nYzs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP825221.RAYWur2yetCqRcDljUlZvEvcS3c1TL2XVIXNdicA-nYzs130_provenance.
- NP825221.RAYWur2yetCqRcDljUlZvEvcS3c1TL2XVIXNdicA-nYzs130_assertion description "[The phenotype of the patient and the expression of SOX3 gene in neuronal tissues raises the possibility that this gene is a candidate gene for Borjeson-Forssman-Lehmann, an X-linked mental retardation syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP825221.RAYWur2yetCqRcDljUlZvEvcS3c1TL2XVIXNdicA-nYzs130_provenance.
- NP825221.RAYWur2yetCqRcDljUlZvEvcS3c1TL2XVIXNdicA-nYzs130_assertion evidence source_evidence_literature NP825221.RAYWur2yetCqRcDljUlZvEvcS3c1TL2XVIXNdicA-nYzs130_provenance.
- NP825221.RAYWur2yetCqRcDljUlZvEvcS3c1TL2XVIXNdicA-nYzs130_assertion SIO_000772 8111369 NP825221.RAYWur2yetCqRcDljUlZvEvcS3c1TL2XVIXNdicA-nYzs130_provenance.
- NP825221.RAYWur2yetCqRcDljUlZvEvcS3c1TL2XVIXNdicA-nYzs130_assertion wasDerivedFrom befree-20140225 NP825221.RAYWur2yetCqRcDljUlZvEvcS3c1TL2XVIXNdicA-nYzs130_provenance.
- NP825221.RAYWur2yetCqRcDljUlZvEvcS3c1TL2XVIXNdicA-nYzs130_assertion wasGeneratedBy ECO_0000203 NP825221.RAYWur2yetCqRcDljUlZvEvcS3c1TL2XVIXNdicA-nYzs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP825221.RAYWur2yetCqRcDljUlZvEvcS3c1TL2XVIXNdicA-nYzs130_provenance.