Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP449457.RAQ6Q3GFwlJDYH_4kqulwHbarVve3J9lXmzW91RxYzaMU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP449457.RAQ6Q3GFwlJDYH_4kqulwHbarVve3J9lXmzW91RxYzaMU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP449457.RAQ6Q3GFwlJDYH_4kqulwHbarVve3J9lXmzW91RxYzaMU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP449457.RAQ6Q3GFwlJDYH_4kqulwHbarVve3J9lXmzW91RxYzaMU130_provenance.
- NP449457.RAQ6Q3GFwlJDYH_4kqulwHbarVve3J9lXmzW91RxYzaMU130_assertion description "[PSMC3IP joins previous genes known to be mutated in XX-GD, the FSH receptor, and BMP15, highlighting the importance of hormonal signaling in ovarian development and maintenance and suggesting a common pathway perturbed in isolated XX-GD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP449457.RAQ6Q3GFwlJDYH_4kqulwHbarVve3J9lXmzW91RxYzaMU130_provenance.
- NP449457.RAQ6Q3GFwlJDYH_4kqulwHbarVve3J9lXmzW91RxYzaMU130_assertion evidence source_evidence_literature NP449457.RAQ6Q3GFwlJDYH_4kqulwHbarVve3J9lXmzW91RxYzaMU130_provenance.
- NP449457.RAQ6Q3GFwlJDYH_4kqulwHbarVve3J9lXmzW91RxYzaMU130_assertion SIO_000772 21963259 NP449457.RAQ6Q3GFwlJDYH_4kqulwHbarVve3J9lXmzW91RxYzaMU130_provenance.
- NP449457.RAQ6Q3GFwlJDYH_4kqulwHbarVve3J9lXmzW91RxYzaMU130_assertion wasDerivedFrom befree-20140225 NP449457.RAQ6Q3GFwlJDYH_4kqulwHbarVve3J9lXmzW91RxYzaMU130_provenance.
- NP449457.RAQ6Q3GFwlJDYH_4kqulwHbarVve3J9lXmzW91RxYzaMU130_assertion wasGeneratedBy ECO_0000203 NP449457.RAQ6Q3GFwlJDYH_4kqulwHbarVve3J9lXmzW91RxYzaMU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP449457.RAQ6Q3GFwlJDYH_4kqulwHbarVve3J9lXmzW91RxYzaMU130_provenance.