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- source_evidence_literature type ECO_0000212 NP412717.RABYk-2UKY0lhk57PoEaAv-bR19xIP5nCIZN2QRr11O2M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP412717.RABYk-2UKY0lhk57PoEaAv-bR19xIP5nCIZN2QRr11O2M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP412717.RABYk-2UKY0lhk57PoEaAv-bR19xIP5nCIZN2QRr11O2M130_provenance.
- NP412717.RABYk-2UKY0lhk57PoEaAv-bR19xIP5nCIZN2QRr11O2M130_assertion description "[A loss-of-function mutation in the FMR1 gene leads to subtle changes in neural development and subsequent mental impairment characteristic of FX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412717.RABYk-2UKY0lhk57PoEaAv-bR19xIP5nCIZN2QRr11O2M130_provenance.
- NP412717.RABYk-2UKY0lhk57PoEaAv-bR19xIP5nCIZN2QRr11O2M130_assertion evidence source_evidence_literature NP412717.RABYk-2UKY0lhk57PoEaAv-bR19xIP5nCIZN2QRr11O2M130_provenance.
- NP412717.RABYk-2UKY0lhk57PoEaAv-bR19xIP5nCIZN2QRr11O2M130_assertion SIO_000772 18225979 NP412717.RABYk-2UKY0lhk57PoEaAv-bR19xIP5nCIZN2QRr11O2M130_provenance.
- NP412717.RABYk-2UKY0lhk57PoEaAv-bR19xIP5nCIZN2QRr11O2M130_assertion wasDerivedFrom befree-20150227 NP412717.RABYk-2UKY0lhk57PoEaAv-bR19xIP5nCIZN2QRr11O2M130_provenance.
- NP412717.RABYk-2UKY0lhk57PoEaAv-bR19xIP5nCIZN2QRr11O2M130_assertion wasGeneratedBy ECO_0000203 NP412717.RABYk-2UKY0lhk57PoEaAv-bR19xIP5nCIZN2QRr11O2M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP412717.RABYk-2UKY0lhk57PoEaAv-bR19xIP5nCIZN2QRr11O2M130_provenance.