Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP864691.RAVbSWrD1uE3RDh2ijTVjHyHXA5RMyiNt_nEK7480C9Uo130_assertion> ?p ?o ?g. }
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- NP864691.RAVbSWrD1uE3RDh2ijTVjHyHXA5RMyiNt_nEK7480C9Uo130_assertion type Assertion NP864691.RAVbSWrD1uE3RDh2ijTVjHyHXA5RMyiNt_nEK7480C9Uo130_head.
- 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.