Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP739052.RA7v2_ngRsB2yfUHCm_8fxDMQD58wAJNHwqt1myDUFFOM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP739052.RA7v2_ngRsB2yfUHCm_8fxDMQD58wAJNHwqt1myDUFFOM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP739052.RA7v2_ngRsB2yfUHCm_8fxDMQD58wAJNHwqt1myDUFFOM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP739052.RA7v2_ngRsB2yfUHCm_8fxDMQD58wAJNHwqt1myDUFFOM130_provenance.
- NP739052.RA7v2_ngRsB2yfUHCm_8fxDMQD58wAJNHwqt1myDUFFOM130_assertion description "[Batten disease (juvenile neuronal ceroid lipofuscinosis, JNCL), the most common neurodegenerative disease of childhood, is caused by mutations in the CLN3 gene encoding a putative transmembrane protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP739052.RA7v2_ngRsB2yfUHCm_8fxDMQD58wAJNHwqt1myDUFFOM130_provenance.
- NP739052.RA7v2_ngRsB2yfUHCm_8fxDMQD58wAJNHwqt1myDUFFOM130_assertion evidence source_evidence_literature NP739052.RA7v2_ngRsB2yfUHCm_8fxDMQD58wAJNHwqt1myDUFFOM130_provenance.
- NP739052.RA7v2_ngRsB2yfUHCm_8fxDMQD58wAJNHwqt1myDUFFOM130_assertion SIO_000772 11590129 NP739052.RA7v2_ngRsB2yfUHCm_8fxDMQD58wAJNHwqt1myDUFFOM130_provenance.
- NP739052.RA7v2_ngRsB2yfUHCm_8fxDMQD58wAJNHwqt1myDUFFOM130_assertion wasDerivedFrom befree-20140225 NP739052.RA7v2_ngRsB2yfUHCm_8fxDMQD58wAJNHwqt1myDUFFOM130_provenance.
- NP739052.RA7v2_ngRsB2yfUHCm_8fxDMQD58wAJNHwqt1myDUFFOM130_assertion wasGeneratedBy ECO_0000203 NP739052.RA7v2_ngRsB2yfUHCm_8fxDMQD58wAJNHwqt1myDUFFOM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP739052.RA7v2_ngRsB2yfUHCm_8fxDMQD58wAJNHwqt1myDUFFOM130_provenance.