Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP422179.RAsnK_I0hw2i9oYC2lfgHP5h2vn08x-fZSQze2szthT3g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP422179.RAsnK_I0hw2i9oYC2lfgHP5h2vn08x-fZSQze2szthT3g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP422179.RAsnK_I0hw2i9oYC2lfgHP5h2vn08x-fZSQze2szthT3g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP422179.RAsnK_I0hw2i9oYC2lfgHP5h2vn08x-fZSQze2szthT3g130_provenance.
- NP422179.RAsnK_I0hw2i9oYC2lfgHP5h2vn08x-fZSQze2szthT3g130_assertion description "[Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP422179.RAsnK_I0hw2i9oYC2lfgHP5h2vn08x-fZSQze2szthT3g130_provenance.
- NP422179.RAsnK_I0hw2i9oYC2lfgHP5h2vn08x-fZSQze2szthT3g130_assertion evidence source_evidence_literature NP422179.RAsnK_I0hw2i9oYC2lfgHP5h2vn08x-fZSQze2szthT3g130_provenance.
- NP422179.RAsnK_I0hw2i9oYC2lfgHP5h2vn08x-fZSQze2szthT3g130_assertion SIO_000772 16645022 NP422179.RAsnK_I0hw2i9oYC2lfgHP5h2vn08x-fZSQze2szthT3g130_provenance.
- NP422179.RAsnK_I0hw2i9oYC2lfgHP5h2vn08x-fZSQze2szthT3g130_assertion wasDerivedFrom befree-20150227 NP422179.RAsnK_I0hw2i9oYC2lfgHP5h2vn08x-fZSQze2szthT3g130_provenance.
- NP422179.RAsnK_I0hw2i9oYC2lfgHP5h2vn08x-fZSQze2szthT3g130_assertion wasGeneratedBy ECO_0000203 NP422179.RAsnK_I0hw2i9oYC2lfgHP5h2vn08x-fZSQze2szthT3g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP422179.RAsnK_I0hw2i9oYC2lfgHP5h2vn08x-fZSQze2szthT3g130_provenance.