Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP553965.RAXXr-mEYVVRoMSOxlwrqqG3c8D9bf1vM7GqtLBBW1bx4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP553965.RAXXr-mEYVVRoMSOxlwrqqG3c8D9bf1vM7GqtLBBW1bx4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP553965.RAXXr-mEYVVRoMSOxlwrqqG3c8D9bf1vM7GqtLBBW1bx4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP553965.RAXXr-mEYVVRoMSOxlwrqqG3c8D9bf1vM7GqtLBBW1bx4130_provenance.
- NP553965.RAXXr-mEYVVRoMSOxlwrqqG3c8D9bf1vM7GqtLBBW1bx4130_assertion description "[In addition, we found an even wider spectrum of reproductive function within pedigrees carrying an FGFR1 mutation ranging from IHH to delayed puberty to normal reproductive function (anosmia only or asymptomatic carriers).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553965.RAXXr-mEYVVRoMSOxlwrqqG3c8D9bf1vM7GqtLBBW1bx4130_provenance.
- NP553965.RAXXr-mEYVVRoMSOxlwrqqG3c8D9bf1vM7GqtLBBW1bx4130_assertion evidence source_evidence_literature NP553965.RAXXr-mEYVVRoMSOxlwrqqG3c8D9bf1vM7GqtLBBW1bx4130_provenance.
- NP553965.RAXXr-mEYVVRoMSOxlwrqqG3c8D9bf1vM7GqtLBBW1bx4130_assertion SIO_000772 16764984 NP553965.RAXXr-mEYVVRoMSOxlwrqqG3c8D9bf1vM7GqtLBBW1bx4130_provenance.
- NP553965.RAXXr-mEYVVRoMSOxlwrqqG3c8D9bf1vM7GqtLBBW1bx4130_assertion wasDerivedFrom befree-2016 NP553965.RAXXr-mEYVVRoMSOxlwrqqG3c8D9bf1vM7GqtLBBW1bx4130_provenance.
- NP553965.RAXXr-mEYVVRoMSOxlwrqqG3c8D9bf1vM7GqtLBBW1bx4130_assertion wasGeneratedBy ECO_0000203 NP553965.RAXXr-mEYVVRoMSOxlwrqqG3c8D9bf1vM7GqtLBBW1bx4130_provenance.
- befree-2016 importedOn "2016-02-19" NP553965.RAXXr-mEYVVRoMSOxlwrqqG3c8D9bf1vM7GqtLBBW1bx4130_provenance.