Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP437970.RATiIBc4nn85id3E8wEx0MQAzGEHDIeam6gZlXfmLB--E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP437970.RATiIBc4nn85id3E8wEx0MQAzGEHDIeam6gZlXfmLB--E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP437970.RATiIBc4nn85id3E8wEx0MQAzGEHDIeam6gZlXfmLB--E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP437970.RATiIBc4nn85id3E8wEx0MQAzGEHDIeam6gZlXfmLB--E130_provenance.
- NP437970.RATiIBc4nn85id3E8wEx0MQAzGEHDIeam6gZlXfmLB--E130_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." NP437970.RATiIBc4nn85id3E8wEx0MQAzGEHDIeam6gZlXfmLB--E130_provenance.
- NP437970.RATiIBc4nn85id3E8wEx0MQAzGEHDIeam6gZlXfmLB--E130_assertion evidence source_evidence_literature NP437970.RATiIBc4nn85id3E8wEx0MQAzGEHDIeam6gZlXfmLB--E130_provenance.
- NP437970.RATiIBc4nn85id3E8wEx0MQAzGEHDIeam6gZlXfmLB--E130_assertion SIO_000772 15057041 NP437970.RATiIBc4nn85id3E8wEx0MQAzGEHDIeam6gZlXfmLB--E130_provenance.
- NP437970.RATiIBc4nn85id3E8wEx0MQAzGEHDIeam6gZlXfmLB--E130_assertion wasDerivedFrom befree-2016 NP437970.RATiIBc4nn85id3E8wEx0MQAzGEHDIeam6gZlXfmLB--E130_provenance.
- NP437970.RATiIBc4nn85id3E8wEx0MQAzGEHDIeam6gZlXfmLB--E130_assertion wasGeneratedBy ECO_0000203 NP437970.RATiIBc4nn85id3E8wEx0MQAzGEHDIeam6gZlXfmLB--E130_provenance.
- befree-2016 importedOn "2016-02-19" NP437970.RATiIBc4nn85id3E8wEx0MQAzGEHDIeam6gZlXfmLB--E130_provenance.