Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP974517.RAjj6GvviEQ8o6_S0SUBfhtEWceKAsMdCo3irNMF6-p9E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP974517.RAjj6GvviEQ8o6_S0SUBfhtEWceKAsMdCo3irNMF6-p9E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP974517.RAjj6GvviEQ8o6_S0SUBfhtEWceKAsMdCo3irNMF6-p9E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP974517.RAjj6GvviEQ8o6_S0SUBfhtEWceKAsMdCo3irNMF6-p9E130_provenance.
- NP974517.RAjj6GvviEQ8o6_S0SUBfhtEWceKAsMdCo3irNMF6-p9E130_assertion description "[Deletion of Xpter encompassing the SHOX gene and PAR1 region in familial patients with Leri-Weill Dyschondrosteosis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP974517.RAjj6GvviEQ8o6_S0SUBfhtEWceKAsMdCo3irNMF6-p9E130_provenance.
- NP974517.RAjj6GvviEQ8o6_S0SUBfhtEWceKAsMdCo3irNMF6-p9E130_assertion evidence source_evidence_literature NP974517.RAjj6GvviEQ8o6_S0SUBfhtEWceKAsMdCo3irNMF6-p9E130_provenance.
- NP974517.RAjj6GvviEQ8o6_S0SUBfhtEWceKAsMdCo3irNMF6-p9E130_assertion SIO_000772 19400538 NP974517.RAjj6GvviEQ8o6_S0SUBfhtEWceKAsMdCo3irNMF6-p9E130_provenance.
- NP974517.RAjj6GvviEQ8o6_S0SUBfhtEWceKAsMdCo3irNMF6-p9E130_assertion wasDerivedFrom befree-20150227 NP974517.RAjj6GvviEQ8o6_S0SUBfhtEWceKAsMdCo3irNMF6-p9E130_provenance.
- NP974517.RAjj6GvviEQ8o6_S0SUBfhtEWceKAsMdCo3irNMF6-p9E130_assertion wasGeneratedBy ECO_0000203 NP974517.RAjj6GvviEQ8o6_S0SUBfhtEWceKAsMdCo3irNMF6-p9E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP974517.RAjj6GvviEQ8o6_S0SUBfhtEWceKAsMdCo3irNMF6-p9E130_provenance.