Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP873848.RAJOtIp5CMZ061w_f_7mhvrzjS8qu5tlxIH0qia_j1eNg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP873848.RAJOtIp5CMZ061w_f_7mhvrzjS8qu5tlxIH0qia_j1eNg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP873848.RAJOtIp5CMZ061w_f_7mhvrzjS8qu5tlxIH0qia_j1eNg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP873848.RAJOtIp5CMZ061w_f_7mhvrzjS8qu5tlxIH0qia_j1eNg130_provenance.
- NP873848.RAJOtIp5CMZ061w_f_7mhvrzjS8qu5tlxIH0qia_j1eNg130_assertion description "[We suggest that L1CAM mutation testing should be considered in male patients with a positive family history compatible with X-linked inheritance and either the combination of agenesis of the CC and HSCR or the combination of agenesis of the CC and limb abnormalities, including abnormalities other than adducted thumbs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873848.RAJOtIp5CMZ061w_f_7mhvrzjS8qu5tlxIH0qia_j1eNg130_provenance.
- NP873848.RAJOtIp5CMZ061w_f_7mhvrzjS8qu5tlxIH0qia_j1eNg130_assertion evidence source_evidence_literature NP873848.RAJOtIp5CMZ061w_f_7mhvrzjS8qu5tlxIH0qia_j1eNg130_provenance.
- NP873848.RAJOtIp5CMZ061w_f_7mhvrzjS8qu5tlxIH0qia_j1eNg130_assertion SIO_000772 16650080 NP873848.RAJOtIp5CMZ061w_f_7mhvrzjS8qu5tlxIH0qia_j1eNg130_provenance.
- NP873848.RAJOtIp5CMZ061w_f_7mhvrzjS8qu5tlxIH0qia_j1eNg130_assertion wasDerivedFrom befree-20140225 NP873848.RAJOtIp5CMZ061w_f_7mhvrzjS8qu5tlxIH0qia_j1eNg130_provenance.
- NP873848.RAJOtIp5CMZ061w_f_7mhvrzjS8qu5tlxIH0qia_j1eNg130_assertion wasGeneratedBy ECO_0000203 NP873848.RAJOtIp5CMZ061w_f_7mhvrzjS8qu5tlxIH0qia_j1eNg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP873848.RAJOtIp5CMZ061w_f_7mhvrzjS8qu5tlxIH0qia_j1eNg130_provenance.