Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP529913.RADCCXukFoSp1KUgA43K_ng81Z9U_aAgCKmiAP0METOQo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP529913.RADCCXukFoSp1KUgA43K_ng81Z9U_aAgCKmiAP0METOQo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP529913.RADCCXukFoSp1KUgA43K_ng81Z9U_aAgCKmiAP0METOQo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP529913.RADCCXukFoSp1KUgA43K_ng81Z9U_aAgCKmiAP0METOQo130_provenance.
- NP529913.RADCCXukFoSp1KUgA43K_ng81Z9U_aAgCKmiAP0METOQo130_assertion description "[We report here the first case of an L1CAM gene mutation identified in mental retardation, adducted thumbs, shuffling gait, and aphasia (MASA) syndrome in Japan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP529913.RADCCXukFoSp1KUgA43K_ng81Z9U_aAgCKmiAP0METOQo130_provenance.
- NP529913.RADCCXukFoSp1KUgA43K_ng81Z9U_aAgCKmiAP0METOQo130_assertion evidence source_evidence_literature NP529913.RADCCXukFoSp1KUgA43K_ng81Z9U_aAgCKmiAP0METOQo130_provenance.
- NP529913.RADCCXukFoSp1KUgA43K_ng81Z9U_aAgCKmiAP0METOQo130_assertion SIO_000772 15904436 NP529913.RADCCXukFoSp1KUgA43K_ng81Z9U_aAgCKmiAP0METOQo130_provenance.
- NP529913.RADCCXukFoSp1KUgA43K_ng81Z9U_aAgCKmiAP0METOQo130_assertion wasDerivedFrom befree-20150227 NP529913.RADCCXukFoSp1KUgA43K_ng81Z9U_aAgCKmiAP0METOQo130_provenance.
- NP529913.RADCCXukFoSp1KUgA43K_ng81Z9U_aAgCKmiAP0METOQo130_assertion wasGeneratedBy ECO_0000203 NP529913.RADCCXukFoSp1KUgA43K_ng81Z9U_aAgCKmiAP0METOQo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP529913.RADCCXukFoSp1KUgA43K_ng81Z9U_aAgCKmiAP0METOQo130_provenance.