Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP862805.RA2FnhW-fBPv4MNZXoIPOOMEJdjtgPDtzfEkiK258KOY8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP862805.RA2FnhW-fBPv4MNZXoIPOOMEJdjtgPDtzfEkiK258KOY8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP862805.RA2FnhW-fBPv4MNZXoIPOOMEJdjtgPDtzfEkiK258KOY8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP862805.RA2FnhW-fBPv4MNZXoIPOOMEJdjtgPDtzfEkiK258KOY8130_provenance.
- NP862805.RA2FnhW-fBPv4MNZXoIPOOMEJdjtgPDtzfEkiK258KOY8130_assertion description "[Rarity of germline 1100delC mutation in CHK2 in patients with malignant melanoma of the skin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862805.RA2FnhW-fBPv4MNZXoIPOOMEJdjtgPDtzfEkiK258KOY8130_provenance.
- NP862805.RA2FnhW-fBPv4MNZXoIPOOMEJdjtgPDtzfEkiK258KOY8130_assertion evidence source_evidence_literature NP862805.RA2FnhW-fBPv4MNZXoIPOOMEJdjtgPDtzfEkiK258KOY8130_provenance.
- NP862805.RA2FnhW-fBPv4MNZXoIPOOMEJdjtgPDtzfEkiK258KOY8130_assertion SIO_000772 15057041 NP862805.RA2FnhW-fBPv4MNZXoIPOOMEJdjtgPDtzfEkiK258KOY8130_provenance.
- NP862805.RA2FnhW-fBPv4MNZXoIPOOMEJdjtgPDtzfEkiK258KOY8130_assertion wasDerivedFrom befree-20150227 NP862805.RA2FnhW-fBPv4MNZXoIPOOMEJdjtgPDtzfEkiK258KOY8130_provenance.
- NP862805.RA2FnhW-fBPv4MNZXoIPOOMEJdjtgPDtzfEkiK258KOY8130_assertion wasGeneratedBy ECO_0000203 NP862805.RA2FnhW-fBPv4MNZXoIPOOMEJdjtgPDtzfEkiK258KOY8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP862805.RA2FnhW-fBPv4MNZXoIPOOMEJdjtgPDtzfEkiK258KOY8130_provenance.