Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP841418.RARbPIAvLY12p4YbbWw6ASdMr2-EACKi_TYa_pdvzKAoU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP841418.RARbPIAvLY12p4YbbWw6ASdMr2-EACKi_TYa_pdvzKAoU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP841418.RARbPIAvLY12p4YbbWw6ASdMr2-EACKi_TYa_pdvzKAoU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP841418.RARbPIAvLY12p4YbbWw6ASdMr2-EACKi_TYa_pdvzKAoU130_provenance.
- NP841418.RARbPIAvLY12p4YbbWw6ASdMr2-EACKi_TYa_pdvzKAoU130_assertion description "[Mutation screening of SEMA3A and SEMA7A in patients with congenital hypogonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841418.RARbPIAvLY12p4YbbWw6ASdMr2-EACKi_TYa_pdvzKAoU130_provenance.
- NP841418.RARbPIAvLY12p4YbbWw6ASdMr2-EACKi_TYa_pdvzKAoU130_assertion evidence source_evidence_literature NP841418.RARbPIAvLY12p4YbbWw6ASdMr2-EACKi_TYa_pdvzKAoU130_provenance.
- NP841418.RARbPIAvLY12p4YbbWw6ASdMr2-EACKi_TYa_pdvzKAoU130_assertion SIO_000772 24522099 NP841418.RARbPIAvLY12p4YbbWw6ASdMr2-EACKi_TYa_pdvzKAoU130_provenance.
- NP841418.RARbPIAvLY12p4YbbWw6ASdMr2-EACKi_TYa_pdvzKAoU130_assertion wasDerivedFrom befree-20150227 NP841418.RARbPIAvLY12p4YbbWw6ASdMr2-EACKi_TYa_pdvzKAoU130_provenance.
- NP841418.RARbPIAvLY12p4YbbWw6ASdMr2-EACKi_TYa_pdvzKAoU130_assertion wasGeneratedBy ECO_0000203 NP841418.RARbPIAvLY12p4YbbWw6ASdMr2-EACKi_TYa_pdvzKAoU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP841418.RARbPIAvLY12p4YbbWw6ASdMr2-EACKi_TYa_pdvzKAoU130_provenance.