Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP844434.RAP-wou3dmhrsFk6TFIDVop-6bakIQHyr2vAukueBVYpY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP844434.RAP-wou3dmhrsFk6TFIDVop-6bakIQHyr2vAukueBVYpY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP844434.RAP-wou3dmhrsFk6TFIDVop-6bakIQHyr2vAukueBVYpY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP844434.RAP-wou3dmhrsFk6TFIDVop-6bakIQHyr2vAukueBVYpY130_provenance.
- NP844434.RAP-wou3dmhrsFk6TFIDVop-6bakIQHyr2vAukueBVYpY130_assertion description "[This patient broadens the spectrum of SLC9A6 mutations and contributes to the clinical delineation of Christianson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844434.RAP-wou3dmhrsFk6TFIDVop-6bakIQHyr2vAukueBVYpY130_provenance.
- NP844434.RAP-wou3dmhrsFk6TFIDVop-6bakIQHyr2vAukueBVYpY130_assertion evidence source_evidence_literature NP844434.RAP-wou3dmhrsFk6TFIDVop-6bakIQHyr2vAukueBVYpY130_provenance.
- NP844434.RAP-wou3dmhrsFk6TFIDVop-6bakIQHyr2vAukueBVYpY130_assertion SIO_000772 21932316 NP844434.RAP-wou3dmhrsFk6TFIDVop-6bakIQHyr2vAukueBVYpY130_provenance.
- NP844434.RAP-wou3dmhrsFk6TFIDVop-6bakIQHyr2vAukueBVYpY130_assertion wasDerivedFrom befree-20150227 NP844434.RAP-wou3dmhrsFk6TFIDVop-6bakIQHyr2vAukueBVYpY130_provenance.
- NP844434.RAP-wou3dmhrsFk6TFIDVop-6bakIQHyr2vAukueBVYpY130_assertion wasGeneratedBy ECO_0000203 NP844434.RAP-wou3dmhrsFk6TFIDVop-6bakIQHyr2vAukueBVYpY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP844434.RAP-wou3dmhrsFk6TFIDVop-6bakIQHyr2vAukueBVYpY130_provenance.