Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1319074.RA9VKLlNm4G8lv7JqWuPcL0sry1FcDIxDXzP47_8n2eTU130_assertion> ?p ?o ?g. }
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- NP1319074.RA9VKLlNm4G8lv7JqWuPcL0sry1FcDIxDXzP47_8n2eTU130_assertion type Assertion NP1319074.RA9VKLlNm4G8lv7JqWuPcL0sry1FcDIxDXzP47_8n2eTU130_head.
- NP1319074.RA9VKLlNm4G8lv7JqWuPcL0sry1FcDIxDXzP47_8n2eTU130_assertion description "[Here we report on a second BFNC family in which linkage to the EBN1 locus on chromosome 20q was excluded, confirming the genetic heterogeneity of this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1319074.RA9VKLlNm4G8lv7JqWuPcL0sry1FcDIxDXzP47_8n2eTU130_provenance.
- NP1319074.RA9VKLlNm4G8lv7JqWuPcL0sry1FcDIxDXzP47_8n2eTU130_assertion evidence source_evidence_literature NP1319074.RA9VKLlNm4G8lv7JqWuPcL0sry1FcDIxDXzP47_8n2eTU130_provenance.
- NP1319074.RA9VKLlNm4G8lv7JqWuPcL0sry1FcDIxDXzP47_8n2eTU130_assertion SIO_000772 7705837 NP1319074.RA9VKLlNm4G8lv7JqWuPcL0sry1FcDIxDXzP47_8n2eTU130_provenance.
- NP1319074.RA9VKLlNm4G8lv7JqWuPcL0sry1FcDIxDXzP47_8n2eTU130_assertion wasDerivedFrom befree-2016 NP1319074.RA9VKLlNm4G8lv7JqWuPcL0sry1FcDIxDXzP47_8n2eTU130_provenance.
- NP1319074.RA9VKLlNm4G8lv7JqWuPcL0sry1FcDIxDXzP47_8n2eTU130_assertion wasGeneratedBy ECO_0000203 NP1319074.RA9VKLlNm4G8lv7JqWuPcL0sry1FcDIxDXzP47_8n2eTU130_provenance.