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- NP616720.RA_oDAfR0icnfQM-Lump0wTLzuyjQgU_8RgoeIhQwfsk0130_assertion type Assertion NP616720.RA_oDAfR0icnfQM-Lump0wTLzuyjQgU_8RgoeIhQwfsk0130_head.
- NP616720.RA_oDAfR0icnfQM-Lump0wTLzuyjQgU_8RgoeIhQwfsk0130_assertion description "[In summary, we conclude that genetic variations in UBQLN2 and PFN1 in a predominantly Flanders-Belgian cohort of FTLD and ALS patients are extremely rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616720.RA_oDAfR0icnfQM-Lump0wTLzuyjQgU_8RgoeIhQwfsk0130_provenance.
- NP616720.RA_oDAfR0icnfQM-Lump0wTLzuyjQgU_8RgoeIhQwfsk0130_assertion evidence source_evidence_literature NP616720.RA_oDAfR0icnfQM-Lump0wTLzuyjQgU_8RgoeIhQwfsk0130_provenance.
- NP616720.RA_oDAfR0icnfQM-Lump0wTLzuyjQgU_8RgoeIhQwfsk0130_assertion SIO_000772 23312802 NP616720.RA_oDAfR0icnfQM-Lump0wTLzuyjQgU_8RgoeIhQwfsk0130_provenance.
- NP616720.RA_oDAfR0icnfQM-Lump0wTLzuyjQgU_8RgoeIhQwfsk0130_assertion wasDerivedFrom befree-20150227 NP616720.RA_oDAfR0icnfQM-Lump0wTLzuyjQgU_8RgoeIhQwfsk0130_provenance.
- NP616720.RA_oDAfR0icnfQM-Lump0wTLzuyjQgU_8RgoeIhQwfsk0130_assertion wasGeneratedBy ECO_0000203 NP616720.RA_oDAfR0icnfQM-Lump0wTLzuyjQgU_8RgoeIhQwfsk0130_provenance.