Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP606391.RA_GjyhT9TNat6fxoxEwjgXkyXC28YlSVjktxMk1hfTWU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP606391.RA_GjyhT9TNat6fxoxEwjgXkyXC28YlSVjktxMk1hfTWU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP606391.RA_GjyhT9TNat6fxoxEwjgXkyXC28YlSVjktxMk1hfTWU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP606391.RA_GjyhT9TNat6fxoxEwjgXkyXC28YlSVjktxMk1hfTWU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP606391.RA_GjyhT9TNat6fxoxEwjgXkyXC28YlSVjktxMk1hfTWU130_provenance.
- NP606391.RA_GjyhT9TNat6fxoxEwjgXkyXC28YlSVjktxMk1hfTWU130_assertion wasGeneratedBy ECO_0000203 NP606391.RA_GjyhT9TNat6fxoxEwjgXkyXC28YlSVjktxMk1hfTWU130_provenance.
- NP606391.RA_GjyhT9TNat6fxoxEwjgXkyXC28YlSVjktxMk1hfTWU130_assertion wasDerivedFrom befree-20150227 NP606391.RA_GjyhT9TNat6fxoxEwjgXkyXC28YlSVjktxMk1hfTWU130_provenance.
- NP606391.RA_GjyhT9TNat6fxoxEwjgXkyXC28YlSVjktxMk1hfTWU130_assertion SIO_000772 7902323 NP606391.RA_GjyhT9TNat6fxoxEwjgXkyXC28YlSVjktxMk1hfTWU130_provenance.
- NP606391.RA_GjyhT9TNat6fxoxEwjgXkyXC28YlSVjktxMk1hfTWU130_assertion evidence source_evidence_literature NP606391.RA_GjyhT9TNat6fxoxEwjgXkyXC28YlSVjktxMk1hfTWU130_provenance.
- NP606391.RA_GjyhT9TNat6fxoxEwjgXkyXC28YlSVjktxMk1hfTWU130_assertion description "[The exclusion of linkage 15 cM on each side of PAH in 16 families with MJD shows that these two forms of dominant ataxia are genetically distinct and at different chromosomal locations (nonallelic).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606391.RA_GjyhT9TNat6fxoxEwjgXkyXC28YlSVjktxMk1hfTWU130_provenance.