Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP864691.RAVbSWrD1uE3RDh2ijTVjHyHXA5RMyiNt_nEK7480C9Uo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP864691.RAVbSWrD1uE3RDh2ijTVjHyHXA5RMyiNt_nEK7480C9Uo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP864691.RAVbSWrD1uE3RDh2ijTVjHyHXA5RMyiNt_nEK7480C9Uo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP864691.RAVbSWrD1uE3RDh2ijTVjHyHXA5RMyiNt_nEK7480C9Uo130_provenance.
- NP864691.RAVbSWrD1uE3RDh2ijTVjHyHXA5RMyiNt_nEK7480C9Uo130_assertion description "[In the present study, we have identified a large number of mutations in SLC17A5 in patients presenting with either Salla disease or the ISSD phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP864691.RAVbSWrD1uE3RDh2ijTVjHyHXA5RMyiNt_nEK7480C9Uo130_provenance.
- NP864691.RAVbSWrD1uE3RDh2ijTVjHyHXA5RMyiNt_nEK7480C9Uo130_assertion evidence source_evidence_literature NP864691.RAVbSWrD1uE3RDh2ijTVjHyHXA5RMyiNt_nEK7480C9Uo130_provenance.
- NP864691.RAVbSWrD1uE3RDh2ijTVjHyHXA5RMyiNt_nEK7480C9Uo130_assertion SIO_000772 10947946 NP864691.RAVbSWrD1uE3RDh2ijTVjHyHXA5RMyiNt_nEK7480C9Uo130_provenance.
- NP864691.RAVbSWrD1uE3RDh2ijTVjHyHXA5RMyiNt_nEK7480C9Uo130_assertion wasDerivedFrom befree-20140225 NP864691.RAVbSWrD1uE3RDh2ijTVjHyHXA5RMyiNt_nEK7480C9Uo130_provenance.
- NP864691.RAVbSWrD1uE3RDh2ijTVjHyHXA5RMyiNt_nEK7480C9Uo130_assertion wasGeneratedBy ECO_0000203 NP864691.RAVbSWrD1uE3RDh2ijTVjHyHXA5RMyiNt_nEK7480C9Uo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP864691.RAVbSWrD1uE3RDh2ijTVjHyHXA5RMyiNt_nEK7480C9Uo130_provenance.