Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP885027.RAKvE4IMisTX0g4rJ1Pjhg1FJJMjdwJ_atEG49Fu3_8K0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP885027.RAKvE4IMisTX0g4rJ1Pjhg1FJJMjdwJ_atEG49Fu3_8K0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP885027.RAKvE4IMisTX0g4rJ1Pjhg1FJJMjdwJ_atEG49Fu3_8K0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP885027.RAKvE4IMisTX0g4rJ1Pjhg1FJJMjdwJ_atEG49Fu3_8K0130_provenance.
- NP885027.RAKvE4IMisTX0g4rJ1Pjhg1FJJMjdwJ_atEG49Fu3_8K0130_assertion description "[Furthermore, we demonstrated increased expression of GRP78 in highly atrophic fibers with pyknotic nuclear clumps in all three muscle biopsies from neurogenic muscular atrophies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP885027.RAKvE4IMisTX0g4rJ1Pjhg1FJJMjdwJ_atEG49Fu3_8K0130_provenance.
- NP885027.RAKvE4IMisTX0g4rJ1Pjhg1FJJMjdwJ_atEG49Fu3_8K0130_assertion evidence source_evidence_literature NP885027.RAKvE4IMisTX0g4rJ1Pjhg1FJJMjdwJ_atEG49Fu3_8K0130_provenance.
- NP885027.RAKvE4IMisTX0g4rJ1Pjhg1FJJMjdwJ_atEG49Fu3_8K0130_assertion SIO_000772 17661063 NP885027.RAKvE4IMisTX0g4rJ1Pjhg1FJJMjdwJ_atEG49Fu3_8K0130_provenance.
- NP885027.RAKvE4IMisTX0g4rJ1Pjhg1FJJMjdwJ_atEG49Fu3_8K0130_assertion wasDerivedFrom befree-20140225 NP885027.RAKvE4IMisTX0g4rJ1Pjhg1FJJMjdwJ_atEG49Fu3_8K0130_provenance.
- NP885027.RAKvE4IMisTX0g4rJ1Pjhg1FJJMjdwJ_atEG49Fu3_8K0130_assertion wasGeneratedBy ECO_0000203 NP885027.RAKvE4IMisTX0g4rJ1Pjhg1FJJMjdwJ_atEG49Fu3_8K0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP885027.RAKvE4IMisTX0g4rJ1Pjhg1FJJMjdwJ_atEG49Fu3_8K0130_provenance.