Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP426933.RA1xHNFA89mrRHF9UwZsjVW3Zegk9VCa9sykBLGWY25yY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP426933.RA1xHNFA89mrRHF9UwZsjVW3Zegk9VCa9sykBLGWY25yY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426933.RA1xHNFA89mrRHF9UwZsjVW3Zegk9VCa9sykBLGWY25yY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426933.RA1xHNFA89mrRHF9UwZsjVW3Zegk9VCa9sykBLGWY25yY130_provenance.
- NP426933.RA1xHNFA89mrRHF9UwZsjVW3Zegk9VCa9sykBLGWY25yY130_assertion description "[The L1CAM gene, which is located in Xq28 and codes for a neuronal cell adhesion molecule, is involved in three distinct conditions: HSAS (hydrocephalus-stenosis of the aqueduct of Sylvius), MASA (mental retardation, aphasia, shuffling gait, adductus thumbs), and SPG1 (spastic paraplegia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426933.RA1xHNFA89mrRHF9UwZsjVW3Zegk9VCa9sykBLGWY25yY130_provenance.
- NP426933.RA1xHNFA89mrRHF9UwZsjVW3Zegk9VCa9sykBLGWY25yY130_assertion evidence source_evidence_literature NP426933.RA1xHNFA89mrRHF9UwZsjVW3Zegk9VCa9sykBLGWY25yY130_provenance.
- NP426933.RA1xHNFA89mrRHF9UwZsjVW3Zegk9VCa9sykBLGWY25yY130_assertion SIO_000772 9744477 NP426933.RA1xHNFA89mrRHF9UwZsjVW3Zegk9VCa9sykBLGWY25yY130_provenance.
- NP426933.RA1xHNFA89mrRHF9UwZsjVW3Zegk9VCa9sykBLGWY25yY130_assertion wasDerivedFrom befree-20140225 NP426933.RA1xHNFA89mrRHF9UwZsjVW3Zegk9VCa9sykBLGWY25yY130_provenance.
- NP426933.RA1xHNFA89mrRHF9UwZsjVW3Zegk9VCa9sykBLGWY25yY130_assertion wasGeneratedBy ECO_0000203 NP426933.RA1xHNFA89mrRHF9UwZsjVW3Zegk9VCa9sykBLGWY25yY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP426933.RA1xHNFA89mrRHF9UwZsjVW3Zegk9VCa9sykBLGWY25yY130_provenance.