Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP811449.RAi2sgvDqSCreHntSDSrDDQ5ZNJ9srrcOOMLx-m_XuabI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP811449.RAi2sgvDqSCreHntSDSrDDQ5ZNJ9srrcOOMLx-m_XuabI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP811449.RAi2sgvDqSCreHntSDSrDDQ5ZNJ9srrcOOMLx-m_XuabI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP811449.RAi2sgvDqSCreHntSDSrDDQ5ZNJ9srrcOOMLx-m_XuabI130_provenance.
- NP811449.RAi2sgvDqSCreHntSDSrDDQ5ZNJ9srrcOOMLx-m_XuabI130_assertion description "[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811449.RAi2sgvDqSCreHntSDSrDDQ5ZNJ9srrcOOMLx-m_XuabI130_provenance.
- NP811449.RAi2sgvDqSCreHntSDSrDDQ5ZNJ9srrcOOMLx-m_XuabI130_assertion evidence source_evidence_literature NP811449.RAi2sgvDqSCreHntSDSrDDQ5ZNJ9srrcOOMLx-m_XuabI130_provenance.
- NP811449.RAi2sgvDqSCreHntSDSrDDQ5ZNJ9srrcOOMLx-m_XuabI130_assertion SIO_000772 17262171 NP811449.RAi2sgvDqSCreHntSDSrDDQ5ZNJ9srrcOOMLx-m_XuabI130_provenance.
- NP811449.RAi2sgvDqSCreHntSDSrDDQ5ZNJ9srrcOOMLx-m_XuabI130_assertion wasDerivedFrom befree-20150227 NP811449.RAi2sgvDqSCreHntSDSrDDQ5ZNJ9srrcOOMLx-m_XuabI130_provenance.
- NP811449.RAi2sgvDqSCreHntSDSrDDQ5ZNJ9srrcOOMLx-m_XuabI130_assertion wasGeneratedBy ECO_0000203 NP811449.RAi2sgvDqSCreHntSDSrDDQ5ZNJ9srrcOOMLx-m_XuabI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP811449.RAi2sgvDqSCreHntSDSrDDQ5ZNJ9srrcOOMLx-m_XuabI130_provenance.