Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP895424.RAEaDqzabDM7e6aIt-zNgUafLOHG3RF8qCJaC0VU1tu1w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP895424.RAEaDqzabDM7e6aIt-zNgUafLOHG3RF8qCJaC0VU1tu1w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP895424.RAEaDqzabDM7e6aIt-zNgUafLOHG3RF8qCJaC0VU1tu1w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP895424.RAEaDqzabDM7e6aIt-zNgUafLOHG3RF8qCJaC0VU1tu1w130_provenance.
- NP895424.RAEaDqzabDM7e6aIt-zNgUafLOHG3RF8qCJaC0VU1tu1w130_assertion description "[Mutations in UBQLN2 encoding ubiquilin-2 have recently been identified in families with dominant X-linked juvenile and adult-onset amyotrophic lateral sclerosis (ALS) and ALS/dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895424.RAEaDqzabDM7e6aIt-zNgUafLOHG3RF8qCJaC0VU1tu1w130_provenance.
- NP895424.RAEaDqzabDM7e6aIt-zNgUafLOHG3RF8qCJaC0VU1tu1w130_assertion evidence source_evidence_literature NP895424.RAEaDqzabDM7e6aIt-zNgUafLOHG3RF8qCJaC0VU1tu1w130_provenance.
- NP895424.RAEaDqzabDM7e6aIt-zNgUafLOHG3RF8qCJaC0VU1tu1w130_assertion SIO_000772 22169395 NP895424.RAEaDqzabDM7e6aIt-zNgUafLOHG3RF8qCJaC0VU1tu1w130_provenance.
- NP895424.RAEaDqzabDM7e6aIt-zNgUafLOHG3RF8qCJaC0VU1tu1w130_assertion wasDerivedFrom befree-20150227 NP895424.RAEaDqzabDM7e6aIt-zNgUafLOHG3RF8qCJaC0VU1tu1w130_provenance.
- NP895424.RAEaDqzabDM7e6aIt-zNgUafLOHG3RF8qCJaC0VU1tu1w130_assertion wasGeneratedBy ECO_0000203 NP895424.RAEaDqzabDM7e6aIt-zNgUafLOHG3RF8qCJaC0VU1tu1w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP895424.RAEaDqzabDM7e6aIt-zNgUafLOHG3RF8qCJaC0VU1tu1w130_provenance.