Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP403816.RAPwE9T7qwgmbJRhXvwPoxlnbo1QvEUWMzg85Ns4xnuPI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP403816.RAPwE9T7qwgmbJRhXvwPoxlnbo1QvEUWMzg85Ns4xnuPI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP403816.RAPwE9T7qwgmbJRhXvwPoxlnbo1QvEUWMzg85Ns4xnuPI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP403816.RAPwE9T7qwgmbJRhXvwPoxlnbo1QvEUWMzg85Ns4xnuPI130_provenance.
- NP403816.RAPwE9T7qwgmbJRhXvwPoxlnbo1QvEUWMzg85Ns4xnuPI130_assertion description "[Patients carrying two reference alleles for the ABCB1 3435C>T polymorphism trended toward a reduced risk to develop neuropathy as compared to patients carrying at least one variant allele (P=0.09).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP403816.RAPwE9T7qwgmbJRhXvwPoxlnbo1QvEUWMzg85Ns4xnuPI130_provenance.
- NP403816.RAPwE9T7qwgmbJRhXvwPoxlnbo1QvEUWMzg85Ns4xnuPI130_assertion evidence source_evidence_literature NP403816.RAPwE9T7qwgmbJRhXvwPoxlnbo1QvEUWMzg85Ns4xnuPI130_provenance.
- NP403816.RAPwE9T7qwgmbJRhXvwPoxlnbo1QvEUWMzg85Ns4xnuPI130_assertion SIO_000772 16950614 NP403816.RAPwE9T7qwgmbJRhXvwPoxlnbo1QvEUWMzg85Ns4xnuPI130_provenance.
- NP403816.RAPwE9T7qwgmbJRhXvwPoxlnbo1QvEUWMzg85Ns4xnuPI130_assertion wasDerivedFrom befree-20140225 NP403816.RAPwE9T7qwgmbJRhXvwPoxlnbo1QvEUWMzg85Ns4xnuPI130_provenance.
- NP403816.RAPwE9T7qwgmbJRhXvwPoxlnbo1QvEUWMzg85Ns4xnuPI130_assertion wasGeneratedBy ECO_0000203 NP403816.RAPwE9T7qwgmbJRhXvwPoxlnbo1QvEUWMzg85Ns4xnuPI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP403816.RAPwE9T7qwgmbJRhXvwPoxlnbo1QvEUWMzg85Ns4xnuPI130_provenance.