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- source_evidence_literature type ECO_0000212 NP207964.RAIG22njNmNnLWnEKTwcSVO93S1zHzUdztBjRc35jqwxo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP207964.RAIG22njNmNnLWnEKTwcSVO93S1zHzUdztBjRc35jqwxo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP207964.RAIG22njNmNnLWnEKTwcSVO93S1zHzUdztBjRc35jqwxo130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP207964.RAIG22njNmNnLWnEKTwcSVO93S1zHzUdztBjRc35jqwxo130_provenance.
- NP207964.RAIG22njNmNnLWnEKTwcSVO93S1zHzUdztBjRc35jqwxo130_assertion wasGeneratedBy ECO_0000203 NP207964.RAIG22njNmNnLWnEKTwcSVO93S1zHzUdztBjRc35jqwxo130_provenance.
- NP207964.RAIG22njNmNnLWnEKTwcSVO93S1zHzUdztBjRc35jqwxo130_assertion wasDerivedFrom lhgdn-20090331 NP207964.RAIG22njNmNnLWnEKTwcSVO93S1zHzUdztBjRc35jqwxo130_provenance.
- NP207964.RAIG22njNmNnLWnEKTwcSVO93S1zHzUdztBjRc35jqwxo130_assertion SIO_000772 15563506 NP207964.RAIG22njNmNnLWnEKTwcSVO93S1zHzUdztBjRc35jqwxo130_provenance.
- NP207964.RAIG22njNmNnLWnEKTwcSVO93S1zHzUdztBjRc35jqwxo130_assertion evidence source_evidence_literature NP207964.RAIG22njNmNnLWnEKTwcSVO93S1zHzUdztBjRc35jqwxo130_provenance.
- NP207964.RAIG22njNmNnLWnEKTwcSVO93S1zHzUdztBjRc35jqwxo130_assertion description "[dominant mutations are common in Ullrich congenital muscular dystrophy (UCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207964.RAIG22njNmNnLWnEKTwcSVO93S1zHzUdztBjRc35jqwxo130_provenance.