Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP974767.RAPt9dFtiqZo0US5DuTXKmUx24xszUoi6BX7pIEQbGI0k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP974767.RAPt9dFtiqZo0US5DuTXKmUx24xszUoi6BX7pIEQbGI0k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP974767.RAPt9dFtiqZo0US5DuTXKmUx24xszUoi6BX7pIEQbGI0k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP974767.RAPt9dFtiqZo0US5DuTXKmUx24xszUoi6BX7pIEQbGI0k130_provenance.
- NP974767.RAPt9dFtiqZo0US5DuTXKmUx24xszUoi6BX7pIEQbGI0k130_assertion description "[This study screened WNT4 for mutation in 189 Chinese women with M�llerian duct abnormalities (10 Mayer-Rokitansky-K�ster-Hauser syndrome, five M�llerian aplasia and 174 incomplete M�llerian fusion) and detected no perturbation that would indicate a major role for WNT4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP974767.RAPt9dFtiqZo0US5DuTXKmUx24xszUoi6BX7pIEQbGI0k130_provenance.
- NP974767.RAPt9dFtiqZo0US5DuTXKmUx24xszUoi6BX7pIEQbGI0k130_assertion evidence source_evidence_literature NP974767.RAPt9dFtiqZo0US5DuTXKmUx24xszUoi6BX7pIEQbGI0k130_provenance.
- NP974767.RAPt9dFtiqZo0US5DuTXKmUx24xszUoi6BX7pIEQbGI0k130_assertion SIO_000772 22503279 NP974767.RAPt9dFtiqZo0US5DuTXKmUx24xszUoi6BX7pIEQbGI0k130_provenance.
- NP974767.RAPt9dFtiqZo0US5DuTXKmUx24xszUoi6BX7pIEQbGI0k130_assertion wasDerivedFrom befree-2016 NP974767.RAPt9dFtiqZo0US5DuTXKmUx24xszUoi6BX7pIEQbGI0k130_provenance.
- NP974767.RAPt9dFtiqZo0US5DuTXKmUx24xszUoi6BX7pIEQbGI0k130_assertion wasGeneratedBy ECO_0000203 NP974767.RAPt9dFtiqZo0US5DuTXKmUx24xszUoi6BX7pIEQbGI0k130_provenance.
- befree-2016 importedOn "2016-02-19" NP974767.RAPt9dFtiqZo0US5DuTXKmUx24xszUoi6BX7pIEQbGI0k130_provenance.