Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP682390.RAgDT38K7OVKRenM2AFMOJ0qv-KLvN52ZTGmgJE1WYBbg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682390.RAgDT38K7OVKRenM2AFMOJ0qv-KLvN52ZTGmgJE1WYBbg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682390.RAgDT38K7OVKRenM2AFMOJ0qv-KLvN52ZTGmgJE1WYBbg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682390.RAgDT38K7OVKRenM2AFMOJ0qv-KLvN52ZTGmgJE1WYBbg130_provenance.
- NP682390.RAgDT38K7OVKRenM2AFMOJ0qv-KLvN52ZTGmgJE1WYBbg130_assertion description "[Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682390.RAgDT38K7OVKRenM2AFMOJ0qv-KLvN52ZTGmgJE1WYBbg130_provenance.
- NP682390.RAgDT38K7OVKRenM2AFMOJ0qv-KLvN52ZTGmgJE1WYBbg130_assertion evidence source_evidence_literature NP682390.RAgDT38K7OVKRenM2AFMOJ0qv-KLvN52ZTGmgJE1WYBbg130_provenance.
- NP682390.RAgDT38K7OVKRenM2AFMOJ0qv-KLvN52ZTGmgJE1WYBbg130_assertion SIO_000772 11799477 NP682390.RAgDT38K7OVKRenM2AFMOJ0qv-KLvN52ZTGmgJE1WYBbg130_provenance.
- NP682390.RAgDT38K7OVKRenM2AFMOJ0qv-KLvN52ZTGmgJE1WYBbg130_assertion wasDerivedFrom befree-20140225 NP682390.RAgDT38K7OVKRenM2AFMOJ0qv-KLvN52ZTGmgJE1WYBbg130_provenance.
- NP682390.RAgDT38K7OVKRenM2AFMOJ0qv-KLvN52ZTGmgJE1WYBbg130_assertion wasGeneratedBy ECO_0000203 NP682390.RAgDT38K7OVKRenM2AFMOJ0qv-KLvN52ZTGmgJE1WYBbg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP682390.RAgDT38K7OVKRenM2AFMOJ0qv-KLvN52ZTGmgJE1WYBbg130_provenance.