Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP172078.RALIoXDh56pV7ax2NwpkWhI8JdXXN9PuDnMsmTYcDjiV4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP172078.RALIoXDh56pV7ax2NwpkWhI8JdXXN9PuDnMsmTYcDjiV4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP172078.RALIoXDh56pV7ax2NwpkWhI8JdXXN9PuDnMsmTYcDjiV4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP172078.RALIoXDh56pV7ax2NwpkWhI8JdXXN9PuDnMsmTYcDjiV4130_provenance.
- NP172078.RALIoXDh56pV7ax2NwpkWhI8JdXXN9PuDnMsmTYcDjiV4130_assertion description "[Different macular dystrophy phenotypes according to the mutations in peripherin/RDS are shown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172078.RALIoXDh56pV7ax2NwpkWhI8JdXXN9PuDnMsmTYcDjiV4130_provenance.
- NP172078.RALIoXDh56pV7ax2NwpkWhI8JdXXN9PuDnMsmTYcDjiV4130_assertion evidence source_evidence_literature NP172078.RALIoXDh56pV7ax2NwpkWhI8JdXXN9PuDnMsmTYcDjiV4130_provenance.
- NP172078.RALIoXDh56pV7ax2NwpkWhI8JdXXN9PuDnMsmTYcDjiV4130_assertion SIO_000772 17653047 NP172078.RALIoXDh56pV7ax2NwpkWhI8JdXXN9PuDnMsmTYcDjiV4130_provenance.
- NP172078.RALIoXDh56pV7ax2NwpkWhI8JdXXN9PuDnMsmTYcDjiV4130_assertion wasDerivedFrom befree-20140225 NP172078.RALIoXDh56pV7ax2NwpkWhI8JdXXN9PuDnMsmTYcDjiV4130_provenance.
- NP172078.RALIoXDh56pV7ax2NwpkWhI8JdXXN9PuDnMsmTYcDjiV4130_assertion wasGeneratedBy ECO_0000203 NP172078.RALIoXDh56pV7ax2NwpkWhI8JdXXN9PuDnMsmTYcDjiV4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP172078.RALIoXDh56pV7ax2NwpkWhI8JdXXN9PuDnMsmTYcDjiV4130_provenance.