Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP429909.RAZWRPZFXk8i4MK56B6BlDAfZQ95112GrZTzDlgTTGVAQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP429909.RAZWRPZFXk8i4MK56B6BlDAfZQ95112GrZTzDlgTTGVAQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP429909.RAZWRPZFXk8i4MK56B6BlDAfZQ95112GrZTzDlgTTGVAQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP429909.RAZWRPZFXk8i4MK56B6BlDAfZQ95112GrZTzDlgTTGVAQ130_provenance.
- NP429909.RAZWRPZFXk8i4MK56B6BlDAfZQ95112GrZTzDlgTTGVAQ130_assertion description "[Familial and sporadic forms of PHP-Ib have distinct GNAS imprinting patterns: familial PHP-Ib patients have an exon A/B-only imprinting defect whereas sporadic PHP-Ib cases have abnormal imprinting of the three differentially methylated regions (DMRs) in GNAS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429909.RAZWRPZFXk8i4MK56B6BlDAfZQ95112GrZTzDlgTTGVAQ130_provenance.
- NP429909.RAZWRPZFXk8i4MK56B6BlDAfZQ95112GrZTzDlgTTGVAQ130_assertion evidence source_evidence_literature NP429909.RAZWRPZFXk8i4MK56B6BlDAfZQ95112GrZTzDlgTTGVAQ130_provenance.
- NP429909.RAZWRPZFXk8i4MK56B6BlDAfZQ95112GrZTzDlgTTGVAQ130_assertion SIO_000772 22300135 NP429909.RAZWRPZFXk8i4MK56B6BlDAfZQ95112GrZTzDlgTTGVAQ130_provenance.
- NP429909.RAZWRPZFXk8i4MK56B6BlDAfZQ95112GrZTzDlgTTGVAQ130_assertion wasDerivedFrom befree-20150227 NP429909.RAZWRPZFXk8i4MK56B6BlDAfZQ95112GrZTzDlgTTGVAQ130_provenance.
- NP429909.RAZWRPZFXk8i4MK56B6BlDAfZQ95112GrZTzDlgTTGVAQ130_assertion wasGeneratedBy ECO_0000203 NP429909.RAZWRPZFXk8i4MK56B6BlDAfZQ95112GrZTzDlgTTGVAQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP429909.RAZWRPZFXk8i4MK56B6BlDAfZQ95112GrZTzDlgTTGVAQ130_provenance.