Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1216025.RApNylrbdtqEd2L-q0-_qCNaasuXZsWqocPFaFEARv3RQ130_assertion> ?p ?o ?g. }
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- NP1216025.RApNylrbdtqEd2L-q0-_qCNaasuXZsWqocPFaFEARv3RQ130_assertion type Assertion NP1216025.RApNylrbdtqEd2L-q0-_qCNaasuXZsWqocPFaFEARv3RQ130_head.
- NP1216025.RApNylrbdtqEd2L-q0-_qCNaasuXZsWqocPFaFEARv3RQ130_assertion description "[This further supports the concept that ALS genes are a rare cause of FTD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216025.RApNylrbdtqEd2L-q0-_qCNaasuXZsWqocPFaFEARv3RQ130_provenance.
- NP1216025.RApNylrbdtqEd2L-q0-_qCNaasuXZsWqocPFaFEARv3RQ130_assertion evidence source_evidence_literature NP1216025.RApNylrbdtqEd2L-q0-_qCNaasuXZsWqocPFaFEARv3RQ130_provenance.
- NP1216025.RApNylrbdtqEd2L-q0-_qCNaasuXZsWqocPFaFEARv3RQ130_assertion SIO_000772 25179229 NP1216025.RApNylrbdtqEd2L-q0-_qCNaasuXZsWqocPFaFEARv3RQ130_provenance.
- NP1216025.RApNylrbdtqEd2L-q0-_qCNaasuXZsWqocPFaFEARv3RQ130_assertion wasDerivedFrom befree-2016 NP1216025.RApNylrbdtqEd2L-q0-_qCNaasuXZsWqocPFaFEARv3RQ130_provenance.
- NP1216025.RApNylrbdtqEd2L-q0-_qCNaasuXZsWqocPFaFEARv3RQ130_assertion wasGeneratedBy ECO_0000203 NP1216025.RApNylrbdtqEd2L-q0-_qCNaasuXZsWqocPFaFEARv3RQ130_provenance.