Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP248802.RA_yCTnxyVYzEJCSHqs6kDNxaCsfLJq_D2lK5n5QX4P8g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP248802.RA_yCTnxyVYzEJCSHqs6kDNxaCsfLJq_D2lK5n5QX4P8g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP248802.RA_yCTnxyVYzEJCSHqs6kDNxaCsfLJq_D2lK5n5QX4P8g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP248802.RA_yCTnxyVYzEJCSHqs6kDNxaCsfLJq_D2lK5n5QX4P8g130_provenance.
- NP248802.RA_yCTnxyVYzEJCSHqs6kDNxaCsfLJq_D2lK5n5QX4P8g130_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." NP248802.RA_yCTnxyVYzEJCSHqs6kDNxaCsfLJq_D2lK5n5QX4P8g130_provenance.
- NP248802.RA_yCTnxyVYzEJCSHqs6kDNxaCsfLJq_D2lK5n5QX4P8g130_assertion evidence source_evidence_literature NP248802.RA_yCTnxyVYzEJCSHqs6kDNxaCsfLJq_D2lK5n5QX4P8g130_provenance.
- NP248802.RA_yCTnxyVYzEJCSHqs6kDNxaCsfLJq_D2lK5n5QX4P8g130_assertion SIO_000772 23524443 NP248802.RA_yCTnxyVYzEJCSHqs6kDNxaCsfLJq_D2lK5n5QX4P8g130_provenance.
- NP248802.RA_yCTnxyVYzEJCSHqs6kDNxaCsfLJq_D2lK5n5QX4P8g130_assertion wasDerivedFrom befree-20150227 NP248802.RA_yCTnxyVYzEJCSHqs6kDNxaCsfLJq_D2lK5n5QX4P8g130_provenance.
- NP248802.RA_yCTnxyVYzEJCSHqs6kDNxaCsfLJq_D2lK5n5QX4P8g130_assertion wasGeneratedBy ECO_0000203 NP248802.RA_yCTnxyVYzEJCSHqs6kDNxaCsfLJq_D2lK5n5QX4P8g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP248802.RA_yCTnxyVYzEJCSHqs6kDNxaCsfLJq_D2lK5n5QX4P8g130_provenance.