Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1062901.RANJhhd7lqCPcq9dg5mgicfV4C3Gt2CJ-qESL7PipZUVs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1062901.RANJhhd7lqCPcq9dg5mgicfV4C3Gt2CJ-qESL7PipZUVs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1062901.RANJhhd7lqCPcq9dg5mgicfV4C3Gt2CJ-qESL7PipZUVs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1062901.RANJhhd7lqCPcq9dg5mgicfV4C3Gt2CJ-qESL7PipZUVs130_provenance.
- NP1062901.RANJhhd7lqCPcq9dg5mgicfV4C3Gt2CJ-qESL7PipZUVs130_assertion description "[Somatic loss of heterozygosity, but not haploinsufficiency alone, leads to full-blown autoimmune lymphoproliferative syndrome in 1 of 12 family members with FAS start codon mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1062901.RANJhhd7lqCPcq9dg5mgicfV4C3Gt2CJ-qESL7PipZUVs130_provenance.
- NP1062901.RANJhhd7lqCPcq9dg5mgicfV4C3Gt2CJ-qESL7PipZUVs130_assertion evidence source_evidence_literature NP1062901.RANJhhd7lqCPcq9dg5mgicfV4C3Gt2CJ-qESL7PipZUVs130_provenance.
- NP1062901.RANJhhd7lqCPcq9dg5mgicfV4C3Gt2CJ-qESL7PipZUVs130_assertion SIO_000772 23524443 NP1062901.RANJhhd7lqCPcq9dg5mgicfV4C3Gt2CJ-qESL7PipZUVs130_provenance.
- NP1062901.RANJhhd7lqCPcq9dg5mgicfV4C3Gt2CJ-qESL7PipZUVs130_assertion wasDerivedFrom befree-2016 NP1062901.RANJhhd7lqCPcq9dg5mgicfV4C3Gt2CJ-qESL7PipZUVs130_provenance.
- NP1062901.RANJhhd7lqCPcq9dg5mgicfV4C3Gt2CJ-qESL7PipZUVs130_assertion wasGeneratedBy ECO_0000203 NP1062901.RANJhhd7lqCPcq9dg5mgicfV4C3Gt2CJ-qESL7PipZUVs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1062901.RANJhhd7lqCPcq9dg5mgicfV4C3Gt2CJ-qESL7PipZUVs130_provenance.