Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP977324.RA4T3o4-PC95wXD0rLr9Qz91XY-Ki1OWv1oPRZVpQlU2E130_assertion> ?p ?o ?g. }
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- NP977324.RA4T3o4-PC95wXD0rLr9Qz91XY-Ki1OWv1oPRZVpQlU2E130_assertion type Assertion NP977324.RA4T3o4-PC95wXD0rLr9Qz91XY-Ki1OWv1oPRZVpQlU2E130_head.
- NP977324.RA4T3o4-PC95wXD0rLr9Qz91XY-Ki1OWv1oPRZVpQlU2E130_assertion description "[More recently, progranulin gene mutations were recognized in association with the familial form of FTLD and a hexanucleotide repetition in C9ORF72 has been shown to be responsible for familial FTLD and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977324.RA4T3o4-PC95wXD0rLr9Qz91XY-Ki1OWv1oPRZVpQlU2E130_provenance.
- NP977324.RA4T3o4-PC95wXD0rLr9Qz91XY-Ki1OWv1oPRZVpQlU2E130_assertion evidence source_evidence_literature NP977324.RA4T3o4-PC95wXD0rLr9Qz91XY-Ki1OWv1oPRZVpQlU2E130_provenance.
- NP977324.RA4T3o4-PC95wXD0rLr9Qz91XY-Ki1OWv1oPRZVpQlU2E130_assertion SIO_000772 22532172 NP977324.RA4T3o4-PC95wXD0rLr9Qz91XY-Ki1OWv1oPRZVpQlU2E130_provenance.
- NP977324.RA4T3o4-PC95wXD0rLr9Qz91XY-Ki1OWv1oPRZVpQlU2E130_assertion wasDerivedFrom befree-2016 NP977324.RA4T3o4-PC95wXD0rLr9Qz91XY-Ki1OWv1oPRZVpQlU2E130_provenance.
- NP977324.RA4T3o4-PC95wXD0rLr9Qz91XY-Ki1OWv1oPRZVpQlU2E130_assertion wasGeneratedBy ECO_0000203 NP977324.RA4T3o4-PC95wXD0rLr9Qz91XY-Ki1OWv1oPRZVpQlU2E130_provenance.