Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP373623.RAlVkEgpquUv4f8abajEFWT_68ULwMWDRSNZumQ-BxyR0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP373623.RAlVkEgpquUv4f8abajEFWT_68ULwMWDRSNZumQ-BxyR0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP373623.RAlVkEgpquUv4f8abajEFWT_68ULwMWDRSNZumQ-BxyR0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP373623.RAlVkEgpquUv4f8abajEFWT_68ULwMWDRSNZumQ-BxyR0130_provenance.
- NP373623.RAlVkEgpquUv4f8abajEFWT_68ULwMWDRSNZumQ-BxyR0130_assertion description "[Lack of fragile X mental retardation protein (FMRP) causes fragile X syndrome, a common form of inherited mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP373623.RAlVkEgpquUv4f8abajEFWT_68ULwMWDRSNZumQ-BxyR0130_provenance.
- NP373623.RAlVkEgpquUv4f8abajEFWT_68ULwMWDRSNZumQ-BxyR0130_assertion evidence source_evidence_literature NP373623.RAlVkEgpquUv4f8abajEFWT_68ULwMWDRSNZumQ-BxyR0130_provenance.
- NP373623.RAlVkEgpquUv4f8abajEFWT_68ULwMWDRSNZumQ-BxyR0130_assertion SIO_000772 12417734 NP373623.RAlVkEgpquUv4f8abajEFWT_68ULwMWDRSNZumQ-BxyR0130_provenance.
- NP373623.RAlVkEgpquUv4f8abajEFWT_68ULwMWDRSNZumQ-BxyR0130_assertion wasDerivedFrom befree-2016 NP373623.RAlVkEgpquUv4f8abajEFWT_68ULwMWDRSNZumQ-BxyR0130_provenance.
- NP373623.RAlVkEgpquUv4f8abajEFWT_68ULwMWDRSNZumQ-BxyR0130_assertion wasGeneratedBy ECO_0000203 NP373623.RAlVkEgpquUv4f8abajEFWT_68ULwMWDRSNZumQ-BxyR0130_provenance.
- befree-2016 importedOn "2016-02-19" NP373623.RAlVkEgpquUv4f8abajEFWT_68ULwMWDRSNZumQ-BxyR0130_provenance.