Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP606695.RANwJ0SoL7YE2p_MMro7jbJjBoJH7yoLO8r0_ZwM8lic8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP606695.RANwJ0SoL7YE2p_MMro7jbJjBoJH7yoLO8r0_ZwM8lic8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP606695.RANwJ0SoL7YE2p_MMro7jbJjBoJH7yoLO8r0_ZwM8lic8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP606695.RANwJ0SoL7YE2p_MMro7jbJjBoJH7yoLO8r0_ZwM8lic8130_provenance.
- NP606695.RANwJ0SoL7YE2p_MMro7jbJjBoJH7yoLO8r0_ZwM8lic8130_assertion description "[If no causative ENG or ACVRL1 mutation is found, proband samples are referred for sequence analysis of MADH4 (associated with a combined syndrome of juvenile polyposis and HHT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606695.RANwJ0SoL7YE2p_MMro7jbJjBoJH7yoLO8r0_ZwM8lic8130_provenance.
- NP606695.RANwJ0SoL7YE2p_MMro7jbJjBoJH7yoLO8r0_ZwM8lic8130_assertion evidence source_evidence_literature NP606695.RANwJ0SoL7YE2p_MMro7jbJjBoJH7yoLO8r0_ZwM8lic8130_provenance.
- NP606695.RANwJ0SoL7YE2p_MMro7jbJjBoJH7yoLO8r0_ZwM8lic8130_assertion SIO_000772 16690726 NP606695.RANwJ0SoL7YE2p_MMro7jbJjBoJH7yoLO8r0_ZwM8lic8130_provenance.
- NP606695.RANwJ0SoL7YE2p_MMro7jbJjBoJH7yoLO8r0_ZwM8lic8130_assertion wasDerivedFrom befree-20140225 NP606695.RANwJ0SoL7YE2p_MMro7jbJjBoJH7yoLO8r0_ZwM8lic8130_provenance.
- NP606695.RANwJ0SoL7YE2p_MMro7jbJjBoJH7yoLO8r0_ZwM8lic8130_assertion wasGeneratedBy ECO_0000203 NP606695.RANwJ0SoL7YE2p_MMro7jbJjBoJH7yoLO8r0_ZwM8lic8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP606695.RANwJ0SoL7YE2p_MMro7jbJjBoJH7yoLO8r0_ZwM8lic8130_provenance.