Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP911248.RAxN1LsqjDpKtRU5GCx6Sr0cIPgAV9m2HlKPRDCZVmS-o130_assertion> ?p ?o ?g. }
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- NP911248.RAxN1LsqjDpKtRU5GCx6Sr0cIPgAV9m2HlKPRDCZVmS-o130_assertion type Assertion NP911248.RAxN1LsqjDpKtRU5GCx6Sr0cIPgAV9m2HlKPRDCZVmS-o130_head.
- NP911248.RAxN1LsqjDpKtRU5GCx6Sr0cIPgAV9m2HlKPRDCZVmS-o130_assertion description "[We conclude that mutations in PFN1 are not a common cause for ALS/FTLD in France.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP911248.RAxN1LsqjDpKtRU5GCx6Sr0cIPgAV9m2HlKPRDCZVmS-o130_provenance.
- NP911248.RAxN1LsqjDpKtRU5GCx6Sr0cIPgAV9m2HlKPRDCZVmS-o130_assertion evidence source_evidence_literature NP911248.RAxN1LsqjDpKtRU5GCx6Sr0cIPgAV9m2HlKPRDCZVmS-o130_provenance.
- NP911248.RAxN1LsqjDpKtRU5GCx6Sr0cIPgAV9m2HlKPRDCZVmS-o130_assertion SIO_000772 23182804 NP911248.RAxN1LsqjDpKtRU5GCx6Sr0cIPgAV9m2HlKPRDCZVmS-o130_provenance.
- NP911248.RAxN1LsqjDpKtRU5GCx6Sr0cIPgAV9m2HlKPRDCZVmS-o130_assertion wasDerivedFrom befree-20140225 NP911248.RAxN1LsqjDpKtRU5GCx6Sr0cIPgAV9m2HlKPRDCZVmS-o130_provenance.
- NP911248.RAxN1LsqjDpKtRU5GCx6Sr0cIPgAV9m2HlKPRDCZVmS-o130_assertion wasGeneratedBy ECO_0000203 NP911248.RAxN1LsqjDpKtRU5GCx6Sr0cIPgAV9m2HlKPRDCZVmS-o130_provenance.