Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP889365.RA38PtFoQMt-H1HH4orkBXWYvcJueJf2V0B-c9qIqg5O4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP889365.RA38PtFoQMt-H1HH4orkBXWYvcJueJf2V0B-c9qIqg5O4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889365.RA38PtFoQMt-H1HH4orkBXWYvcJueJf2V0B-c9qIqg5O4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889365.RA38PtFoQMt-H1HH4orkBXWYvcJueJf2V0B-c9qIqg5O4130_provenance.
- NP889365.RA38PtFoQMt-H1HH4orkBXWYvcJueJf2V0B-c9qIqg5O4130_assertion wasGeneratedBy ECO_0000203 NP889365.RA38PtFoQMt-H1HH4orkBXWYvcJueJf2V0B-c9qIqg5O4130_provenance.
- NP889365.RA38PtFoQMt-H1HH4orkBXWYvcJueJf2V0B-c9qIqg5O4130_assertion wasDerivedFrom befree-20140225 NP889365.RA38PtFoQMt-H1HH4orkBXWYvcJueJf2V0B-c9qIqg5O4130_provenance.
- NP889365.RA38PtFoQMt-H1HH4orkBXWYvcJueJf2V0B-c9qIqg5O4130_assertion SIO_000772 17855450 NP889365.RA38PtFoQMt-H1HH4orkBXWYvcJueJf2V0B-c9qIqg5O4130_provenance.
- NP889365.RA38PtFoQMt-H1HH4orkBXWYvcJueJf2V0B-c9qIqg5O4130_assertion evidence source_evidence_literature NP889365.RA38PtFoQMt-H1HH4orkBXWYvcJueJf2V0B-c9qIqg5O4130_provenance.
- NP889365.RA38PtFoQMt-H1HH4orkBXWYvcJueJf2V0B-c9qIqg5O4130_assertion description "[Mutations in Alsin are associated with chronic juvenile amyotrophic lateral sclerosis (ALS2), juvenile primary lateral sclerosis and infantile-onset ascending spastic paralysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889365.RA38PtFoQMt-H1HH4orkBXWYvcJueJf2V0B-c9qIqg5O4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP889365.RA38PtFoQMt-H1HH4orkBXWYvcJueJf2V0B-c9qIqg5O4130_provenance.