Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP153536.RATKIV1vecIs-Dn7PGxovCWG18E72kdw0pAtbLP3PClII130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP153536.RATKIV1vecIs-Dn7PGxovCWG18E72kdw0pAtbLP3PClII130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP153536.RATKIV1vecIs-Dn7PGxovCWG18E72kdw0pAtbLP3PClII130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP153536.RATKIV1vecIs-Dn7PGxovCWG18E72kdw0pAtbLP3PClII130_provenance.
- NP153536.RATKIV1vecIs-Dn7PGxovCWG18E72kdw0pAtbLP3PClII130_assertion description "[Mutations cause X-linked Coffin-Lowry Syndrome, a mental retardation syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153536.RATKIV1vecIs-Dn7PGxovCWG18E72kdw0pAtbLP3PClII130_provenance.
- NP153536.RATKIV1vecIs-Dn7PGxovCWG18E72kdw0pAtbLP3PClII130_assertion evidence source_evidence_literature NP153536.RATKIV1vecIs-Dn7PGxovCWG18E72kdw0pAtbLP3PClII130_provenance.
- NP153536.RATKIV1vecIs-Dn7PGxovCWG18E72kdw0pAtbLP3PClII130_assertion SIO_000772 11896450 NP153536.RATKIV1vecIs-Dn7PGxovCWG18E72kdw0pAtbLP3PClII130_provenance.
- NP153536.RATKIV1vecIs-Dn7PGxovCWG18E72kdw0pAtbLP3PClII130_assertion wasDerivedFrom lhgdn-20090331 NP153536.RATKIV1vecIs-Dn7PGxovCWG18E72kdw0pAtbLP3PClII130_provenance.
- NP153536.RATKIV1vecIs-Dn7PGxovCWG18E72kdw0pAtbLP3PClII130_assertion wasGeneratedBy ECO_0000203 NP153536.RATKIV1vecIs-Dn7PGxovCWG18E72kdw0pAtbLP3PClII130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP153536.RATKIV1vecIs-Dn7PGxovCWG18E72kdw0pAtbLP3PClII130_provenance.