Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP437970.RATiIBc4nn85id3E8wEx0MQAzGEHDIeam6gZlXfmLB--E130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP437970.RATiIBc4nn85id3E8wEx0MQAzGEHDIeam6gZlXfmLB--E130_assertion type Assertion NP437970.RATiIBc4nn85id3E8wEx0MQAzGEHDIeam6gZlXfmLB--E130_head.
- 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.