Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_provenance.
- NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_assertion description "[The authors report detailed clinical and developmental assessment of 3 brothers who were found to carry a novel mutation in the ARX gene associated with a relatively mild phenotype of static global developmental delay and early hand preference.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_provenance.
- NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_assertion evidence source_evidence_literature NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_provenance.
- NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_assertion SIO_000772 22922607 NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_provenance.
- NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_assertion wasDerivedFrom befree-20150227 NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_provenance.
- NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_assertion wasGeneratedBy ECO_0000203 NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_provenance.