Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP962967.RAyF_1GidWGP4tDDevDzbgl5qEBYwPZgMSKWqs_mFovi0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP962967.RAyF_1GidWGP4tDDevDzbgl5qEBYwPZgMSKWqs_mFovi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP962967.RAyF_1GidWGP4tDDevDzbgl5qEBYwPZgMSKWqs_mFovi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP962967.RAyF_1GidWGP4tDDevDzbgl5qEBYwPZgMSKWqs_mFovi0130_provenance.
- NP962967.RAyF_1GidWGP4tDDevDzbgl5qEBYwPZgMSKWqs_mFovi0130_assertion description "[Substantial efforts have been deployed in the past decade to identify the genetic causes of amyotrophic lateral sclerosis (ALS), and we hypothesized here that mutations in SORT1 or aberrant SORT1 splicing reduce progranulin level and promote neurodegeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP962967.RAyF_1GidWGP4tDDevDzbgl5qEBYwPZgMSKWqs_mFovi0130_provenance.
- NP962967.RAyF_1GidWGP4tDDevDzbgl5qEBYwPZgMSKWqs_mFovi0130_assertion evidence source_evidence_literature NP962967.RAyF_1GidWGP4tDDevDzbgl5qEBYwPZgMSKWqs_mFovi0130_provenance.
- NP962967.RAyF_1GidWGP4tDDevDzbgl5qEBYwPZgMSKWqs_mFovi0130_assertion SIO_000772 22361451 NP962967.RAyF_1GidWGP4tDDevDzbgl5qEBYwPZgMSKWqs_mFovi0130_provenance.
- NP962967.RAyF_1GidWGP4tDDevDzbgl5qEBYwPZgMSKWqs_mFovi0130_assertion wasDerivedFrom befree-2016 NP962967.RAyF_1GidWGP4tDDevDzbgl5qEBYwPZgMSKWqs_mFovi0130_provenance.
- NP962967.RAyF_1GidWGP4tDDevDzbgl5qEBYwPZgMSKWqs_mFovi0130_assertion wasGeneratedBy ECO_0000203 NP962967.RAyF_1GidWGP4tDDevDzbgl5qEBYwPZgMSKWqs_mFovi0130_provenance.
- befree-2016 importedOn "2016-02-19" NP962967.RAyF_1GidWGP4tDDevDzbgl5qEBYwPZgMSKWqs_mFovi0130_provenance.