Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP901357.RA9B6Y9F0pQaeTSm7546O-W3lgTN2O4u41biLiP1fRk4g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP901357.RA9B6Y9F0pQaeTSm7546O-W3lgTN2O4u41biLiP1fRk4g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP901357.RA9B6Y9F0pQaeTSm7546O-W3lgTN2O4u41biLiP1fRk4g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP901357.RA9B6Y9F0pQaeTSm7546O-W3lgTN2O4u41biLiP1fRk4g130_provenance.
- NP901357.RA9B6Y9F0pQaeTSm7546O-W3lgTN2O4u41biLiP1fRk4g130_assertion description "[The data confirm the pathologic significance of SPG4 mutations in pure ADHSP and add to the list of known SPG4 allelic variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP901357.RA9B6Y9F0pQaeTSm7546O-W3lgTN2O4u41biLiP1fRk4g130_provenance.
- NP901357.RA9B6Y9F0pQaeTSm7546O-W3lgTN2O4u41biLiP1fRk4g130_assertion evidence source_evidence_literature NP901357.RA9B6Y9F0pQaeTSm7546O-W3lgTN2O4u41biLiP1fRk4g130_provenance.
- NP901357.RA9B6Y9F0pQaeTSm7546O-W3lgTN2O4u41biLiP1fRk4g130_assertion SIO_000772 10980739 NP901357.RA9B6Y9F0pQaeTSm7546O-W3lgTN2O4u41biLiP1fRk4g130_provenance.
- NP901357.RA9B6Y9F0pQaeTSm7546O-W3lgTN2O4u41biLiP1fRk4g130_assertion wasDerivedFrom befree-20140225 NP901357.RA9B6Y9F0pQaeTSm7546O-W3lgTN2O4u41biLiP1fRk4g130_provenance.
- NP901357.RA9B6Y9F0pQaeTSm7546O-W3lgTN2O4u41biLiP1fRk4g130_assertion wasGeneratedBy ECO_0000203 NP901357.RA9B6Y9F0pQaeTSm7546O-W3lgTN2O4u41biLiP1fRk4g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP901357.RA9B6Y9F0pQaeTSm7546O-W3lgTN2O4u41biLiP1fRk4g130_provenance.