Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP831010.RA266BKZgptVWmcuPDKUEcsgblQHRCrrDbOwh3dEtnRF4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP831010.RA266BKZgptVWmcuPDKUEcsgblQHRCrrDbOwh3dEtnRF4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831010.RA266BKZgptVWmcuPDKUEcsgblQHRCrrDbOwh3dEtnRF4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831010.RA266BKZgptVWmcuPDKUEcsgblQHRCrrDbOwh3dEtnRF4130_provenance.
- NP831010.RA266BKZgptVWmcuPDKUEcsgblQHRCrrDbOwh3dEtnRF4130_assertion description "[These results allow further delineation of the spectrum of malformations ascribed to SMADIP1 haploinsufficiency, which includes frequent features such as hypospadias and agenesis of the corpus callosum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831010.RA266BKZgptVWmcuPDKUEcsgblQHRCrrDbOwh3dEtnRF4130_provenance.
- NP831010.RA266BKZgptVWmcuPDKUEcsgblQHRCrrDbOwh3dEtnRF4130_assertion evidence source_evidence_literature NP831010.RA266BKZgptVWmcuPDKUEcsgblQHRCrrDbOwh3dEtnRF4130_provenance.
- NP831010.RA266BKZgptVWmcuPDKUEcsgblQHRCrrDbOwh3dEtnRF4130_assertion SIO_000772 11595972 NP831010.RA266BKZgptVWmcuPDKUEcsgblQHRCrrDbOwh3dEtnRF4130_provenance.
- NP831010.RA266BKZgptVWmcuPDKUEcsgblQHRCrrDbOwh3dEtnRF4130_assertion wasDerivedFrom befree-20150227 NP831010.RA266BKZgptVWmcuPDKUEcsgblQHRCrrDbOwh3dEtnRF4130_provenance.
- NP831010.RA266BKZgptVWmcuPDKUEcsgblQHRCrrDbOwh3dEtnRF4130_assertion wasGeneratedBy ECO_0000203 NP831010.RA266BKZgptVWmcuPDKUEcsgblQHRCrrDbOwh3dEtnRF4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP831010.RA266BKZgptVWmcuPDKUEcsgblQHRCrrDbOwh3dEtnRF4130_provenance.