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- source_evidence_literature type ECO_0000212 NP938259.RAcCzg-c5Y2_ZJWJclyPOdIolb30VOuTzHxJan_0xKJpU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP938259.RAcCzg-c5Y2_ZJWJclyPOdIolb30VOuTzHxJan_0xKJpU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP938259.RAcCzg-c5Y2_ZJWJclyPOdIolb30VOuTzHxJan_0xKJpU130_provenance.
- NP938259.RAcCzg-c5Y2_ZJWJclyPOdIolb30VOuTzHxJan_0xKJpU130_assertion description "[VCP mutations in familial and sporadic amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP938259.RAcCzg-c5Y2_ZJWJclyPOdIolb30VOuTzHxJan_0xKJpU130_provenance.
- NP938259.RAcCzg-c5Y2_ZJWJclyPOdIolb30VOuTzHxJan_0xKJpU130_assertion evidence source_evidence_literature NP938259.RAcCzg-c5Y2_ZJWJclyPOdIolb30VOuTzHxJan_0xKJpU130_provenance.
- NP938259.RAcCzg-c5Y2_ZJWJclyPOdIolb30VOuTzHxJan_0xKJpU130_assertion SIO_000772 22078486 NP938259.RAcCzg-c5Y2_ZJWJclyPOdIolb30VOuTzHxJan_0xKJpU130_provenance.
- NP938259.RAcCzg-c5Y2_ZJWJclyPOdIolb30VOuTzHxJan_0xKJpU130_assertion wasDerivedFrom befree-2016 NP938259.RAcCzg-c5Y2_ZJWJclyPOdIolb30VOuTzHxJan_0xKJpU130_provenance.
- NP938259.RAcCzg-c5Y2_ZJWJclyPOdIolb30VOuTzHxJan_0xKJpU130_assertion wasGeneratedBy ECO_0000203 NP938259.RAcCzg-c5Y2_ZJWJclyPOdIolb30VOuTzHxJan_0xKJpU130_provenance.
- befree-2016 importedOn "2016-02-19" NP938259.RAcCzg-c5Y2_ZJWJclyPOdIolb30VOuTzHxJan_0xKJpU130_provenance.