Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP140629.RA1su7EPOdQVWFH5i4pugEvgMfZu4Iao_qoLgj-MFBNl4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP140629.RA1su7EPOdQVWFH5i4pugEvgMfZu4Iao_qoLgj-MFBNl4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP140629.RA1su7EPOdQVWFH5i4pugEvgMfZu4Iao_qoLgj-MFBNl4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP140629.RA1su7EPOdQVWFH5i4pugEvgMfZu4Iao_qoLgj-MFBNl4130_provenance.
- NP140629.RA1su7EPOdQVWFH5i4pugEvgMfZu4Iao_qoLgj-MFBNl4130_assertion description "[identification of missense mutations in FUS in familial amyotrophic lateral sclerosis type 6; expression studies revealed aberrant localization of mutant FUS protein ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP140629.RA1su7EPOdQVWFH5i4pugEvgMfZu4Iao_qoLgj-MFBNl4130_provenance.
- NP140629.RA1su7EPOdQVWFH5i4pugEvgMfZu4Iao_qoLgj-MFBNl4130_assertion evidence source_evidence_literature NP140629.RA1su7EPOdQVWFH5i4pugEvgMfZu4Iao_qoLgj-MFBNl4130_provenance.
- NP140629.RA1su7EPOdQVWFH5i4pugEvgMfZu4Iao_qoLgj-MFBNl4130_assertion SIO_000772 19251628 NP140629.RA1su7EPOdQVWFH5i4pugEvgMfZu4Iao_qoLgj-MFBNl4130_provenance.
- NP140629.RA1su7EPOdQVWFH5i4pugEvgMfZu4Iao_qoLgj-MFBNl4130_assertion wasDerivedFrom lhgdn-20090331 NP140629.RA1su7EPOdQVWFH5i4pugEvgMfZu4Iao_qoLgj-MFBNl4130_provenance.
- NP140629.RA1su7EPOdQVWFH5i4pugEvgMfZu4Iao_qoLgj-MFBNl4130_assertion wasGeneratedBy ECO_0000203 NP140629.RA1su7EPOdQVWFH5i4pugEvgMfZu4Iao_qoLgj-MFBNl4130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP140629.RA1su7EPOdQVWFH5i4pugEvgMfZu4Iao_qoLgj-MFBNl4130_provenance.