Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1319074.RA9VKLlNm4G8lv7JqWuPcL0sry1FcDIxDXzP47_8n2eTU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1319074.RA9VKLlNm4G8lv7JqWuPcL0sry1FcDIxDXzP47_8n2eTU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1319074.RA9VKLlNm4G8lv7JqWuPcL0sry1FcDIxDXzP47_8n2eTU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1319074.RA9VKLlNm4G8lv7JqWuPcL0sry1FcDIxDXzP47_8n2eTU130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1319074.RA9VKLlNm4G8lv7JqWuPcL0sry1FcDIxDXzP47_8n2eTU130_provenance.