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- source_evidence_literature type ECO_0000212 NP303981.RASZ47pHKXqyvsO0wfJdSHsPD-XrR_lO0mRZPk_9WYG_c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP303981.RASZ47pHKXqyvsO0wfJdSHsPD-XrR_lO0mRZPk_9WYG_c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP303981.RASZ47pHKXqyvsO0wfJdSHsPD-XrR_lO0mRZPk_9WYG_c130_provenance.
- NP303981.RASZ47pHKXqyvsO0wfJdSHsPD-XrR_lO0mRZPk_9WYG_c130_assertion description "[To the best of our knowledge this is the first report of CDKN1C mutations in children born to women with preeclampsia/HELLP syndrome, thus suggesting the involvement of an imprinted gene in the pathophysiology of preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP303981.RASZ47pHKXqyvsO0wfJdSHsPD-XrR_lO0mRZPk_9WYG_c130_provenance.
- NP303981.RASZ47pHKXqyvsO0wfJdSHsPD-XrR_lO0mRZPk_9WYG_c130_assertion evidence source_evidence_literature NP303981.RASZ47pHKXqyvsO0wfJdSHsPD-XrR_lO0mRZPk_9WYG_c130_provenance.
- NP303981.RASZ47pHKXqyvsO0wfJdSHsPD-XrR_lO0mRZPk_9WYG_c130_assertion SIO_000772 19386358 NP303981.RASZ47pHKXqyvsO0wfJdSHsPD-XrR_lO0mRZPk_9WYG_c130_provenance.
- NP303981.RASZ47pHKXqyvsO0wfJdSHsPD-XrR_lO0mRZPk_9WYG_c130_assertion wasDerivedFrom befree-20150227 NP303981.RASZ47pHKXqyvsO0wfJdSHsPD-XrR_lO0mRZPk_9WYG_c130_provenance.
- NP303981.RASZ47pHKXqyvsO0wfJdSHsPD-XrR_lO0mRZPk_9WYG_c130_assertion wasGeneratedBy ECO_0000203 NP303981.RASZ47pHKXqyvsO0wfJdSHsPD-XrR_lO0mRZPk_9WYG_c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP303981.RASZ47pHKXqyvsO0wfJdSHsPD-XrR_lO0mRZPk_9WYG_c130_provenance.