Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP631535.RA_MyE89Z11SA9NLbCiC84zQykw1cqoavbU6yDAauFnUw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP631535.RA_MyE89Z11SA9NLbCiC84zQykw1cqoavbU6yDAauFnUw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP631535.RA_MyE89Z11SA9NLbCiC84zQykw1cqoavbU6yDAauFnUw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP631535.RA_MyE89Z11SA9NLbCiC84zQykw1cqoavbU6yDAauFnUw130_provenance.
- NP631535.RA_MyE89Z11SA9NLbCiC84zQykw1cqoavbU6yDAauFnUw130_assertion description "[The phenotypic presentation in five patients was suggestive of a complex HSP that associated an early-onset spastic paraplegia with mild handicap, mental deterioration, congenital cataract, cerebellar signs, and TCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP631535.RA_MyE89Z11SA9NLbCiC84zQykw1cqoavbU6yDAauFnUw130_provenance.
- NP631535.RA_MyE89Z11SA9NLbCiC84zQykw1cqoavbU6yDAauFnUw130_assertion evidence source_evidence_literature NP631535.RA_MyE89Z11SA9NLbCiC84zQykw1cqoavbU6yDAauFnUw130_provenance.
- NP631535.RA_MyE89Z11SA9NLbCiC84zQykw1cqoavbU6yDAauFnUw130_assertion SIO_000772 20593214 NP631535.RA_MyE89Z11SA9NLbCiC84zQykw1cqoavbU6yDAauFnUw130_provenance.
- NP631535.RA_MyE89Z11SA9NLbCiC84zQykw1cqoavbU6yDAauFnUw130_assertion wasDerivedFrom befree-20140225 NP631535.RA_MyE89Z11SA9NLbCiC84zQykw1cqoavbU6yDAauFnUw130_provenance.
- NP631535.RA_MyE89Z11SA9NLbCiC84zQykw1cqoavbU6yDAauFnUw130_assertion wasGeneratedBy ECO_0000203 NP631535.RA_MyE89Z11SA9NLbCiC84zQykw1cqoavbU6yDAauFnUw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP631535.RA_MyE89Z11SA9NLbCiC84zQykw1cqoavbU6yDAauFnUw130_provenance.