Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP303128.RAj2-LILG9gfH41toN9LPZboqO8yRIwqzwJhz00z0lBSo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP303128.RAj2-LILG9gfH41toN9LPZboqO8yRIwqzwJhz00z0lBSo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP303128.RAj2-LILG9gfH41toN9LPZboqO8yRIwqzwJhz00z0lBSo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP303128.RAj2-LILG9gfH41toN9LPZboqO8yRIwqzwJhz00z0lBSo130_provenance.
- NP303128.RAj2-LILG9gfH41toN9LPZboqO8yRIwqzwJhz00z0lBSo130_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." NP303128.RAj2-LILG9gfH41toN9LPZboqO8yRIwqzwJhz00z0lBSo130_provenance.
- NP303128.RAj2-LILG9gfH41toN9LPZboqO8yRIwqzwJhz00z0lBSo130_assertion evidence source_evidence_literature NP303128.RAj2-LILG9gfH41toN9LPZboqO8yRIwqzwJhz00z0lBSo130_provenance.
- NP303128.RAj2-LILG9gfH41toN9LPZboqO8yRIwqzwJhz00z0lBSo130_assertion SIO_000772 21963259 NP303128.RAj2-LILG9gfH41toN9LPZboqO8yRIwqzwJhz00z0lBSo130_provenance.
- NP303128.RAj2-LILG9gfH41toN9LPZboqO8yRIwqzwJhz00z0lBSo130_assertion wasDerivedFrom befree-20140225 NP303128.RAj2-LILG9gfH41toN9LPZboqO8yRIwqzwJhz00z0lBSo130_provenance.
- NP303128.RAj2-LILG9gfH41toN9LPZboqO8yRIwqzwJhz00z0lBSo130_assertion wasGeneratedBy ECO_0000203 NP303128.RAj2-LILG9gfH41toN9LPZboqO8yRIwqzwJhz00z0lBSo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP303128.RAj2-LILG9gfH41toN9LPZboqO8yRIwqzwJhz00z0lBSo130_provenance.