Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3449.RA1mUqh33xv-csfI9NSbx6W23otIn_4ra9hq8WvAXtyEk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP3449.RA1mUqh33xv-csfI9NSbx6W23otIn_4ra9hq8WvAXtyEk130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3449.RA1mUqh33xv-csfI9NSbx6W23otIn_4ra9hq8WvAXtyEk130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3449.RA1mUqh33xv-csfI9NSbx6W23otIn_4ra9hq8WvAXtyEk130_provenance.
- NP3449.RA1mUqh33xv-csfI9NSbx6W23otIn_4ra9hq8WvAXtyEk130_assertion description "[The autosomal recessive skeletal dysplasia known as acromesomelic dysplasia, type Maroteaux (AMDM) maps to an interval that contains NPR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3449.RA1mUqh33xv-csfI9NSbx6W23otIn_4ra9hq8WvAXtyEk130_provenance.
- NP3449.RA1mUqh33xv-csfI9NSbx6W23otIn_4ra9hq8WvAXtyEk130_assertion evidence source_evidence_curated NP3449.RA1mUqh33xv-csfI9NSbx6W23otIn_4ra9hq8WvAXtyEk130_provenance.
- NP3449.RA1mUqh33xv-csfI9NSbx6W23otIn_4ra9hq8WvAXtyEk130_assertion SIO_000772 15146390 NP3449.RA1mUqh33xv-csfI9NSbx6W23otIn_4ra9hq8WvAXtyEk130_provenance.
- NP3449.RA1mUqh33xv-csfI9NSbx6W23otIn_4ra9hq8WvAXtyEk130_assertion wasDerivedFrom uniprot-2016 NP3449.RA1mUqh33xv-csfI9NSbx6W23otIn_4ra9hq8WvAXtyEk130_provenance.
- NP3449.RA1mUqh33xv-csfI9NSbx6W23otIn_4ra9hq8WvAXtyEk130_assertion wasGeneratedBy ECO_0000218 NP3449.RA1mUqh33xv-csfI9NSbx6W23otIn_4ra9hq8WvAXtyEk130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP3449.RA1mUqh33xv-csfI9NSbx6W23otIn_4ra9hq8WvAXtyEk130_provenance.