Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP868620.RAbtFQ8gj_5dvPF26yKYkjE8zpDCQyR416uhCR9ZSvOwk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP868620.RAbtFQ8gj_5dvPF26yKYkjE8zpDCQyR416uhCR9ZSvOwk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868620.RAbtFQ8gj_5dvPF26yKYkjE8zpDCQyR416uhCR9ZSvOwk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868620.RAbtFQ8gj_5dvPF26yKYkjE8zpDCQyR416uhCR9ZSvOwk130_provenance.
- NP868620.RAbtFQ8gj_5dvPF26yKYkjE8zpDCQyR416uhCR9ZSvOwk130_assertion description "[Mutations in the p63 gene have recently been delineated as the molecular basis for some cases of the ectrodactyly, ectodermal dysplasia and cleft lip/palate (EEC) syndrome, an autosomal dominant disorder (MIM 129900).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868620.RAbtFQ8gj_5dvPF26yKYkjE8zpDCQyR416uhCR9ZSvOwk130_provenance.
- NP868620.RAbtFQ8gj_5dvPF26yKYkjE8zpDCQyR416uhCR9ZSvOwk130_assertion evidence source_evidence_literature NP868620.RAbtFQ8gj_5dvPF26yKYkjE8zpDCQyR416uhCR9ZSvOwk130_provenance.
- NP868620.RAbtFQ8gj_5dvPF26yKYkjE8zpDCQyR416uhCR9ZSvOwk130_assertion SIO_000772 11012604 NP868620.RAbtFQ8gj_5dvPF26yKYkjE8zpDCQyR416uhCR9ZSvOwk130_provenance.
- NP868620.RAbtFQ8gj_5dvPF26yKYkjE8zpDCQyR416uhCR9ZSvOwk130_assertion wasDerivedFrom befree-20140225 NP868620.RAbtFQ8gj_5dvPF26yKYkjE8zpDCQyR416uhCR9ZSvOwk130_provenance.
- NP868620.RAbtFQ8gj_5dvPF26yKYkjE8zpDCQyR416uhCR9ZSvOwk130_assertion wasGeneratedBy ECO_0000203 NP868620.RAbtFQ8gj_5dvPF26yKYkjE8zpDCQyR416uhCR9ZSvOwk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP868620.RAbtFQ8gj_5dvPF26yKYkjE8zpDCQyR416uhCR9ZSvOwk130_provenance.