Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP904001.RAhmKn_OmT7-om2hnvZNSoAKZCtp_zsZ4NIk846s11Voc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP904001.RAhmKn_OmT7-om2hnvZNSoAKZCtp_zsZ4NIk846s11Voc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP904001.RAhmKn_OmT7-om2hnvZNSoAKZCtp_zsZ4NIk846s11Voc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP904001.RAhmKn_OmT7-om2hnvZNSoAKZCtp_zsZ4NIk846s11Voc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP904001.RAhmKn_OmT7-om2hnvZNSoAKZCtp_zsZ4NIk846s11Voc130_provenance.
- NP904001.RAhmKn_OmT7-om2hnvZNSoAKZCtp_zsZ4NIk846s11Voc130_assertion wasGeneratedBy ECO_0000203 NP904001.RAhmKn_OmT7-om2hnvZNSoAKZCtp_zsZ4NIk846s11Voc130_provenance.
- NP904001.RAhmKn_OmT7-om2hnvZNSoAKZCtp_zsZ4NIk846s11Voc130_assertion wasDerivedFrom befree-20150227 NP904001.RAhmKn_OmT7-om2hnvZNSoAKZCtp_zsZ4NIk846s11Voc130_provenance.
- NP904001.RAhmKn_OmT7-om2hnvZNSoAKZCtp_zsZ4NIk846s11Voc130_assertion SIO_000772 11311134 NP904001.RAhmKn_OmT7-om2hnvZNSoAKZCtp_zsZ4NIk846s11Voc130_provenance.
- NP904001.RAhmKn_OmT7-om2hnvZNSoAKZCtp_zsZ4NIk846s11Voc130_assertion evidence source_evidence_literature NP904001.RAhmKn_OmT7-om2hnvZNSoAKZCtp_zsZ4NIk846s11Voc130_provenance.
- NP904001.RAhmKn_OmT7-om2hnvZNSoAKZCtp_zsZ4NIk846s11Voc130_assertion description "[These results suggest that BM88 may be a candidate gene for genetic disorders associated with alterations at 11p15.5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP904001.RAhmKn_OmT7-om2hnvZNSoAKZCtp_zsZ4NIk846s11Voc130_provenance.